Method of preparing pregelatinized, partially hydrolyzed starch and related methods and products

ABSTRACT

Disclosed are methods relating to an extruded pregelatinized, partially hydrolyzed starch prepared by mixing at least water, non-pregelatinized starch, and acid to form a starch precursor. The acid can be a weak acid that substantially avoids chelating calcium ions or a strong acid in a small amount. In the method, pregelatinization and acid-modification of the starch precursor occurs in one step in an extruder. Also disclosed are methods of preparing board using the starch prepared according to the methods, as well as starches and boards prepared by various methods of the invention.

CROSS-REFERENCE TO RELATED APPLICATIONS

This patent application is a continuation of copending U.S. patentapplication Ser. No. 14/494,547, filed Sep. 23, 2014, which is acontinuation-in-part of U.S. patent application Ser. No. 14/044,582,filed Oct. 2, 2013, now U.S. Pat. No. 9,540,810, which is acontinuation-in-part of copending U.S. patent application Ser. No.13/835,002, filed Mar. 15, 2013, which claims the benefit of U.S.Provisional Patent Application No. 61/717,588, filed Oct. 23, 2012, allof which preceding patent applications are incorporated herein byreference in their entireties.

BACKGROUND OF THE INVENTION

Starches generally contain two types of polysaccharides (amylose andamylopectin) and are classified as carbohydrates. Some starches arepregelatinized, typically through thermal means. Generally,pregelatinized starches can form dispersions, pastes, or gels with coldwater. Pregelatinized starches are generally digestible and have beenused in a number of ways, including as an additive to a variety of foodproducts (e.g., in baking, snacks, beverages, confections, dairy,gravies, prepared foods, sauces, and meats) and in pharmaceuticals.

Another use for pregelatinized starches is in the preparation of gypsumwallboard. In this regard, during manufacture of the board, stucco(i.e., calcined gypsum in the form of calcium sulfate hemihydrate and/orcalcium sulfate anhydrite), water, starch, and other ingredients asappropriate are mixed, typically in a pin mixer as the term is used inthe art. A slurry is formed and discharged from the mixer onto a movingconveyor carrying a cover sheet with one of the skim coats (if present)already applied (often upstream of the mixer). The slurry is spread overthe paper (with skim coat optionally included on the paper). Anothercover sheet, with or without skim coat, is applied onto the slurry toform the sandwich structure of desired thickness with the aid of, e.g.,a forming plate or the like.

The mixture is cast and allowed to harden to form set (i.e., rehydrated)gypsum by reaction of the calcined gypsum with water to form a matrix ofcrystalline hydrated gypsum (i.e., calcium sulfate dihydrate). It is thedesired hydration of the calcined gypsum that enables the formation ofthe interlocking matrix of set gypsum crystals, thereby impartingstrength to the gypsum structure in the product. Heat is required (e.g.,in a kiln) to drive off the remaining free (i.e., unreacted) water toyield a dry product.

Often, pregelatinized starches add water demand to the process. Tocompensate for the water demand and allow for sufficient fluidity duringmanufacture, water content must be added into the stucco slurry. Thisexcess water creates inefficiencies in the manufacture, includingincreased drying time, slower manufacturing line speeds, and higherenergy costs. The inventors have found that pregelatinized and partiallyhydrolyzed starch demands less water.

The inventors have also found that techniques for preparingpregelatinized, partially hydrolyzed starches have not been fullysatisfactory. Conventional methods for preparing such pregelatinized,partially hydrolyzed starches have not been efficient, with low outputand slow production, as well as high energy costs. Thus, there is a needin the art for an improved method of preparing pregelatinized, partiallyhydrolyzed starch, particularly exhibiting low water demand.

It will be appreciated that this background description has been createdby the inventors to aid the reader, and is not to be taken as areference to prior art nor as an indication that any of the indicatedproblems were themselves appreciated in the art. While the describedprinciples can, in some regards and embodiments, alleviate the problemsinherent in other systems, it will be appreciated that the scope of theprotected innovation is defined by the attached claims, and not by theability of the claimed invention to solve any specific problem notedherein.

BRIEF SUMMARY OF THE INVENTION

In one aspect, the invention provides a method of making apregelatinized, partially hydrolyzed starch comprising: (a) mixing atleast water, non-pregelatinized starch, and a weak acid thatsubstantially avoids chelating calcium ions to make a wet starchprecursor having a moisture content of from about 8 wt. % to about 25wt. %; (b) feeding the wet starch precursor into an extruder; and (c)pregelatinizing and acid-modifying the wet starch precursor in theextruder at a die temperature of about 150° C. (about 300° F.) to about210° C. (about 410° F.). The invention also provides a starch producedaccording to this method.

In another aspect, the invention provides a method of making apregelatinized, partially hydrolyzed starch comprising: (a) mixing atleast water, non-pregelatinized starch, and a strong acid to make a wetstarch precursor having a moisture content of from about 8 wt. % toabout 25 wt. %, wherein the strong acid is in an amount of about 0.05wt. % or less by weight of the starch; (b) feeding the wet starch intoan extruder; and (c) pregelatinizing and acid-modifying the wet starchprecursor in the extruder at a die temperature of about 150° C. (about300° F.) to about 210° C. (about 410° F.). The invention also provides astarch produced according to this method.

In another aspect, the invention provides a method of making boardcomprising: (a) forming a pregelatinized, partially hydrolyzed starch by(i) mixing at least water, non-pregelatinized starch, and an acid toform a wet starch precursor having a moisture content of from about 8wt. % to about 25 wt. %, the acid selected from the group consisting of:(1) a weak acid that substantially avoids chelating calcium ions, (2) astrong acid in an amount of about 0.05 wt. % or less by weight of thestarch, or (3) any combination thereof; (ii) feeding the wet starchprecursor into an extruder, and (iii) pregelatinizing and acid-modifyingthe wet starch in the extruder having a die at a temperature of about150° C. (about 300° F.) to about 210° C. (about 410° F.); (b) mixing thepregelatinized and partially hydrolyzed starch with at least water andstucco to form a slurry; (c) disposing the slurry between a first coversheet and a second cover sheet to form a wet assembly; (d) cutting thewet assembly into a board; and (e) drying the board. In someembodiments, the set gypsum core has a compressive strength greater thana set gypsum core made with a starch prepared under a different method.In another aspect, the invention provides a board produced according tothis method.

BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWINGS

FIG. 1 is an amylogram plotting viscosity (left y-axis) and temperature(right y-axis) versus time (x-axis) that shows pasting profiles ofstarches extruded at a moisture content of 16 wt. % with the solidcontent of testing slurry being 10 wt. % as set forth in Example 2.

FIG. 2 is an amylogram plotting viscosity (left y-axis) and temperature(right y-axis) versus time (x-axis) that shows pasting profiles ofstarches extruded at a moisture content of 13 wt. % with the solidcontent of testing slurry being 10 wt. % as set forth in Example 2.

FIG. 3 is a graph plotting temperature versus time showing thetemperature rise set (TRS) hydration rate of two slurries containingpregelatinized, partially hydrolyzed starches treated with alum in anamount of 3 wt. % and retarder in amounts of 0.05 wt. % and 0.0625 wt.%, respectively, and a third slurry containing a conventionalpregelatinized corn starch having a viscosity of 773 centipoise andretarder in an amount of 0.05 wt. % as set forth in Example 3.

DETAILED DESCRIPTION OF THE INVENTION

Embodiments of the invention provide methods of making pregelatinized,partially hydrolyzed starches. In one aspect, the invention provides amethod of preparing board (e.g., gypsum wallboard). Pregelatinized,partially hydrolyzed starches produced according to the method of theinvention can be used in a variety of other ways, such as in foodstuffs(e.g., in baked goods, beverages, confections, dairy, instant puddings,gravies, soup mixes, prepared foods, pie fillings, sauces, and meats),pharmaceuticals, feeds, adhesives, and colorings. Such starches preparedin accordance with some embodiments of the invention are generallydigestible and can provide food products with desired viscosity, and canretain most of the functional properties of the original base material.

Embodiments of the invention are premised, at least in part, on thesurprising and unexpected discovery of pregelatinizing andacid-modifying starch in a single step in an extruder. Surprisingly andunexpectedly, pregelatinizing and acid-modifying starch in a single stepin an extruder has considerable advantages in comparison topregelatinizing and acid-modifying starch in separate steps. Forexample, the inventive method of making pregelatinized, partiallyhydrolyzed starch allows for a higher output, faster production, andlower energy costs without sacrificing desired properties (e.g.,viscosity, fluidity, cold water solubility, etc.) as described herein.

In addition, it has been found that the extrusion conditions (e.g., hightemperature and high pressure) can significantly increase the acidhydrolysis rate of starch. Surprisingly and unexpectedly, this singlestep process makes possible using a weak acid, such as alum, and/orsmaller amounts of strong acid, for starch acid-modification. Eitheracid form provides a mechanism where protons from acids catalyze thehydrolysis of starch. Conventional acid-modification processes includepurification and neutralization steps. The use of a weak acid (e.g.,alum) and/or a small amount of a strong acid avoids the need for anyneutralization step and the subsequent purification step typicallyrequired in conventional systems to purify the starch of salts resultingfrom the neutralization step, in accordance with some embodiments of theinvention.

The extrusion process, in accordance with embodiments of the invention,not only pregelatinizes the starch, but also partially hydrolyzes (i.e.,via acid-modification) starch molecules. Thus, the extrusion process inone step provides both physical modification (pregelatinization) andchemical modification (acid-modification, partially acid hydrolysis).The pregelatinization provides the ability for the starch to impartstrength (e.g., on a final product such as gypsum board).Acid-modification beneficially partially hydrolyzes the starch toprovide the starch with the ability to impart strength on a finalproduct, such as gypsum board, and low water demand in productmanufacture, such as in the case of gypsum board manufacturingprocesses. Thus, the product of methods of preparing starch inaccordance with embodiments of the invention is pregelatinized andpartially hydrolyzed starch.

In accordance with some embodiments, the invention provides a highlyefficient acid-modification reaction. The pregelatinization andacid-modification in the extruder occurs at elevated temperatures and/orpressures as described herein and can result in an acid hydrolysis ratethat can be, e.g., approximately 30,000 times or greater faster thanconventional acid hydrolysis rates at lower temperatures (e.g., 50° C.)and/or pressures. The rate of acid hydrolysis is further increasedthrough the use of low moisture (about 8 wt. % to about 25 wt. %) levelsin the starch precursor and hence through an increased concentration ofreactants. Because of this high efficiency of acid-modification, theinventors have found that, surprisingly and unexpectedly, a weak acid ora very low level of strong acid can be used in the starch precursor toachieve optimal acid-modification and avoid the need for neutralizationand purification which are costly, time consuming, and inefficientrequirements of conventional systems.

In accordance with some embodiments, the hydrolysis is designed toconvert the starch into smaller molecules within an optimum size range,which is defined herein by the desired viscosity of the pregelatinized,partially hydrolyzed starch. If the starch is over hydrolyzed, it can beconverted into unduly small molecules (e.g., oligosaccharides orsugars), which, in the case of gypsum board, can result in less boardstrength than that provided by the pregelatinized, partially hydrolyzedstarch of desired viscosity.

The pregelatinized, partially hydrolyzed starch can be prepared by (i)mixing at least water, non-pregelatinized starch, and an acid to form awet starch precursor having a moisture content of from about 8 wt. % toabout 25 wt. %. The acid can be: (1) a weak acid that substantiallyavoids chelating calcium ions, (2) a strong acid in an amount of about0.05 wt. % or less by weight of the starch, or (3) any combinationthereof. The wet starch precursor is pregelatinized and acid-modified inone step in an extruder at an elevated die temperature and/or pressureas described herein. The starch is hydrolyzed to a degree that resultsin a desired viscosity, e.g., as described herein.

Thus, in some embodiments, a pregelatinized, partially hydrolyzed starchcan be made by mixing at least water, non-pregelatinized starch, and aweak acid that substantially avoids chelating calcium ions to make a wetstarch precursor having a moisture content of from about 8 wt. % toabout 25 wt. %. The wet starch is then fed into an extruder. While inthe extruder at a die temperature of about 150° C. (about 300° F.) toabout 210° C. (about 410° F.), the wet starch is pregelatinized andacid-modified, such that it is at least partially hydrolyzed.

In further embodiments, a pregelatinized, partially hydrolyzed starchcan be made by mixing at least water, non-pregelatinized starch, and astrong acid to make a wet starch precursor having a moisture content offrom about 8 wt. % to about 25 wt. %, wherein the strong acid is in anamount of about 0.05 wt. % or less by weight of the starch. The wetstarch is then fed into an extruder. While in the extruder at a dietemperature of about 150° C. (about 300° F.) to about 210° C. (about410° F.), the wet starch is pregelatinized and acid-modified, such thatit is at least partially hydrolyzed.

Desirably, the resulting pregelatinized, partially hydrolyzed starch haslow water demand when included in a stucco slurry and can be useful inthe manufacture of board (e.g., gypsum board) with good strength, insome embodiments. Thus, in another aspect, the invention provides amethod of making gypsum board using starch prepared with the inventivemethods of pregelatinizing and acid-modifying in a single step in anextruder. In some embodiments, the pregelatinized, partially hydrolyzedstarches prepared in accordance with embodiments of the invention havelow water demand relative to other pregelatinized starches known in theart.

As a result, pregelatinized, partially hydrolyzed starches prepared inaccordance with embodiments of the invention can be included in a stuccoslurry (e.g., by a feed line into a pin mixer) with good fluidity. Insome embodiments, higher amounts of the pregelatinized, partiallyhydrolyzed starches prepared in accordance with embodiments of theinvention can be included since excess water is not needed to be addedto the system, such that even higher strengths and lower board densitiescan be achieved. The resulting board exhibits good strength properties(e.g., having good core hardness, nail pull resistance, compressivestrength, etc., or any relationship therebetween, based on anycombination of values for each provided herein). Advantageously,inclusion of starch prepared according to the method of the inventionduring the manufacture of gypsum board enables the production of ultralow density product because of the strength enhancements. The gypsumboard can be in the form of, e.g., gypsum wallboard (often referred toas drywall), which can encompass such board used not only for walls butalso for ceilings and other locations as understood in the art. However,starch prepared according to the method can have other applications,such as in food products.

Pregelatinization and Acid-Modification

Starches are classified as carbohydrates and contain two types ofpolysaccharides, namely linear amylose, and branched amylopectin. Starchgranules are semi-crystalline, e.g., as seen under polarized light, andare insoluble at room temperatures. Gelatinization is the process bywhich the starch is placed in water and heated (“cooked”), such that thecrystalline structure of the starch granules is melted, and the starchmolecules are dissolved in water, resulting in good dispersion. It hasbeen found that, when transforming a starch granule to gelatinized form,initially, the starch granule provides little viscosity in water becausestarch granules are water insoluble. As the temperature increases, thestarch granule swells and the crystalline structure melts at thegelatinization temperature. Peak viscosity is achieved when the starchgranule has maximum swelling. Further heating will break the starchgranules and dissolve the starch molecules in water, with a precipitousdrop-off in viscosity. After cooling, the starch molecule willre-associate to form a 3-D gel structure, with the viscosity increasingdue to the gel structure. Some commercial starches are sold in apregelatinized form, while others are sold in the granular form. Inaccordance with some embodiments of the present invention, in relationto gypsum board, the granular form undergoes at least some degree ofgelatinization. To illustrate, in relation to gypsum board, the starchis pregelatinized prior to its addition to gypsum slurry, also referredto herein as stucco slurry (typically in a mixer, e.g., a pin mixer).

Thus, as used herein, “pregelatinized” means that the starch has anydegree of gelatinization, e.g., before it is included in the gypsumslurry or for use in other applications. In some embodiments relating togypsum board, the pregelatinized starch can be partially gelatinizedwhen included in the slurry, but becomes fully gelatinized when exposedto elevated temperature, e.g., in the kiln during the drying step toremove excess water. In some embodiments relating to gypsum board, thepregelatinized starch is not fully gelatinized, even upon exiting thekiln so long as the starch meets the mid-range viscosity characteristicof some embodiments when under the conditions according to the ViscosityModifying Admixture (VMA) method.

When viscosity is referred to herein, it is in accordance with the VMAmethod, unless otherwise indicated. According to this method, viscosityis measured using a Discovery HR-2 Hybrid Rheometer (TA Instruments Ltd)with a concentric cylinder, a standard cup (diameter of 30 mm) with vanegeometry (diameter of 28 mm and length of 42.05 mm).

When the starch is obtained, differential scanning calorimetry (DSC)techniques are used to determine whether the starch is fullygelatinized. The DSC step can be utilized to observe whether starch isfully gelatinized, e.g., to confirm that no retrogradation has occurred.One of two procedures is adopted, depending on the temperature requiredto fully gelatinize the starch, which can also be determined by DSC asone of ordinary skill in the art will appreciate.

Procedure 1 is utilized where the DSC reveals that the starch is fullygelatinized or has a gelatinization temperature at or below 90° C.Procedure 2 is utilized where the gelatinization temperature is above90° C. Since the viscosity is measured while the starch is in water,procedure 2 uses pressure cooking in a sealed vessel to allow forsuperheating to temperatures above 100° C. without causing the water toappreciably evaporate. Procedure 1 is reserved for starches alreadyfully gelatinized or for starches having gelatinization temperature upto 90° C., because, as discussed below, the gelatinization takes placein the rheometer which is an open system and cannot create pressurizedconditions for gelatinization. Thus procedure 2 is followed for starcheshaving higher gelatinization temperatures. Either way, starch (7.5 g,dry basis) is added into water for a total weight of 50 g when theviscosity is measured.

In procedure 1, the starch is dispersed in the water (15% starch of thetotal weight of starch and water) and the sample is immediatelytransferred to a cylinder cell. The cell is covered with aluminum foil.The sample is heated from 25° C. to 90° C. at 5° C./imin and a shearrate of 200 s⁻¹. The sample is held at 90° C. for 10 min at a shear rateof 200 s⁻¹. The sample is cooled from 90° C. to 80° C. at 5° C./min anda shear rate of 200 s⁻¹. The sample is held at 80° C. for 10 min at ashear rate of 0 s⁻¹. The viscosity of the sample is measured at 80° C.and a shear rate of 100 s⁻¹ for 2 min. The viscosity is the average ofthe measurement from 30 seconds to 60 seconds.

Procedure 2 is used for starches having gelatinization temperaturegreater than 90° C. The starch is gelatinized according to the methodswell-known in the starch industry (e.g., by pressure cooking). Thegelatinized starch water solution (15% of total weight) is immediatelytransferred into the rheometer measuring cup and equilibrated at 80° C.for 10 minutes. The viscosity of the sample is measured at 80° C. and ashear rate of 100 s⁻¹ for 2 minutes. The viscosity is the average of themeasurement from 30 seconds to 60 seconds.

Viscograph and DSC are two different methods to describe starchgelatinization. Degree of starch gelatinization can be determined by,for example, thermogram from DSC, e.g., using peak area (melting ofcrystal) for calculation. A viscogram (from viscograph) is lessdesirable to determine degree of partial gelatinization but is a goodtool to obtain data such as the viscosity change of starch,gelatinization maximum, gelatinization temperature, retrogradation,viscosity during holding, viscosity at the end of cooling, etc. Fordegree of gelatinization, the DSC measurements are done in the presenceof excess water, particularly at or above 67% by weight. If watercontent of starch/water mixture is less than 67%, gelatinizationtemperature will increase as water content decreases. It is difficult tomelt starch crystals when available water is limited. When water contentof starch/water mixture reaches 67%, gelatinization temperature willkeep constant no matter how much more water is added into the starch,water mixture. Gelatinization onset temperature indicates the startingtemperature of gelatinization. Gelatinization end temperature indicatesthe end temperature of gelatinization. Enthalpy of gelatinizationrepresents the amount of crystalline structure melted duringgelatinization. By using the enthalpy from a starch DSC thermogram, thedegree of gelatinization can be indicated.

Different starches have different gelatinization onset temperatures, endtemperatures, and gelatinization enthalpies. Therefore, differentstarches may become fully gelatinized at different temperatures. It willbe understood that a starch is fully gelatinized when the starch isheated beyond the end temperature of gelatinization in excess water. Inaddition, for any particular starch, if the starch is heated below theend temperature of gelatinization, the starch will be partiallygelatinized. Thus, partial and not full gelatinization will occur whenstarch in the presence of excess water is heated below gelatinizationend temperature, e.g., as determined by DSC. Full gelatinization willoccur when starch in the presence of excess water is heated abovegelatinization end temperature, e.g., as determined by DSC. The degreeof gelatinization can be adjusted in different ways, such as, forexample, by heating the starch below the gelatinization end temperatureto form partial gelatinization. For example, if the enthalpy for fullygelatinizing a starch is 4 J/g, when the DSC shows the gelatinizationenthalpy of the starch as being only 2 Jig, this means 50% of the starchhas been gelatinized. Fully gelatinized starch would not have the DSCthermogram gelatinization peak (enthalpy=0 J/g) when it is measured byDSC.

As noted, the degree of gelatinization can be any suitable amount, suchas about 70% or more, etc. However, smaller degrees of gelatinizationwill more closely approximate granular starch and may not take fulladvantage of the strength enhancement, better (more complete)dispersion, and/or water demand reduction of some embodiments of theinvention. Thus, in some embodiments, it is preferred that there is ahigher degree of gelatinization, e.g., at least about 75%, at leastabout 80%, at least about 85%, at least about 90%, at least about 95%,at least about 97%, at least about 99%, or full (100%) gelatinization.Starch with lower degree of gelatinization can be added to slurry withadditional gelatinization (e.g., to 100%) taking place in the kiln inthe case of gypsum board. For purposes of addition to slurry, by “fullygelatinized,” it will be understood that the starch is sufficientlycooked at or above its gelatinization temperature or to otherwiseachieve full gelatinization as can be seen from DSC techniques. Althoughsome small degree of retrogradation upon cooling may be expected, thestarch will still be understood as “fully gelatinized” for addition togypsum slurry, or for use in other applications, in some embodiments asone of ordinary skill in the art will recognize. In contrast, forpurposes of the VMA method discussed herein, such retrogradation is notaccepted in making the viscosity measurement.

The starch molecule can be acid-modified, e.g., to hydrolyze glycosidicbonds between glucose units to achieve desired molecular weight. Onebenefit of acid-modifying starch such that a reduction in molecularweight is achieved is that the water demand will decrease. Conventionalpregelatinized starches that were not also acid-modified had a very highwater demand, which is associated with higher energy costs. It has beenconventionally believed that it is generally preferred that themodification take place before gelatinization because it tends to bemore efficient and less cost intensive. Surprisingly and unexpectedly,however, the inventors have found that pregelatinization andacid-modification can be incorporated into a single step, such that theycan occur simultaneously rather than in series.

Method of Preparing Starch

In accordance with some embodiments of the invention, prior to entryinto the extruder, a wet starch precursor is prepared. The wet starchprecursor can be prepared by any suitable method. For example, in someembodiments, the wet starch precursor is prepared by adding to a starchraw material water and an acid that is (a) a weak acid thatsubstantially avoids chelating calcium ions, and/or (b) a strong acid ina small amount.

Any suitable starch raw material can be selected to prepare the wetstarch precursor so long as it can be used to make pregelatinized,partially hydrolyzed starch, such as one meeting the mid-range viscositycharacteristic of some embodiments of the invention. As used herein,“starch” refers to a composition that includes a starch component. Assuch, the starch can be 100% pure starch or may have other componentssuch as those commonly found in flours such as protein and fiber, solong as the starch component makes up at least about 75% by weight ofthe starch composition. The starch can be in the form of a flour (e.g.,corn flour) containing starch, such as flour having at least about 75%starch by weight of the flour, e.g., at least about 80%, at least about85%, at least about 90%, at least about 95%, etc.). Any suitableunmodified starch or flour can be used to prepare the precursor of thepregelatinized, partially hydrolyzed starches of the invention. Forexample, the starch can be CCM260 yellow corn meal, CCF600 yellow cornflour (Bunge North America), Clinton 106 (ADM), and/or Midsol 50 (MGPIngredients).

The wet starch precursor can be prepared to have any suitable moisturecontent, such that desired levels of pregelatinization andacid-modification are achieved in an extruder. In some embodiments, forexample, it is desirable that the wet starch precursor have a moisturecontent of from about 8 wt. % to about 25 wt. % by weight of the totalstarch precursor, such as from about 8 wt. % to about 23 wt. %, e.g.,from about 8 wt. % to about 21 wt. %, from about 8 wt. % to about 20 wt.%, from about 8 wt. % to about 19 wt. %, from about 8 wt. % to about 18wt. %, from about 8 wt. % to about 17 wt. %, from about 8 wt. % to about16 wt. %, from about 8 wt. % to about 15 wt. %, from about 9 wt. % toabout 25 wt. %, from about 9 wt. % to about 23 wt. %, from about 9 wt. %to about 21 wt. %, from about 9 wt. % to about 20 wt. %, from about 9wt. % to about 19 wt. %, from about 9 wt. % to about 18 wt. %, fromabout 9 wt. % to about 17 wt. %, from about 9 wt. % to about 16 wt. %,from about 9 wt. % to about 15 wt. %, from about 10 wt. % to about 25wt. %, from about 10 wt. % to about 23 wt. %, from about 10 wt. % toabout 21 wt. %, from about 10 wt. % to about 20 wt. %, from about 10 wt.% to about 19 wt. %, from about 10 wt. % to about 18 wt. %, from about10 wt. % to about 17 wt. %, from about 10 wt. % to about 16 wt. %, fromabout 10 wt. % to about 15 wt. %, from about 11 wt. % to about 25 wt. %,from about 11 wt. % to about 23 wt. %, from about 11 wt. % to about 21wt. %, from about 11 wt. % to about 20 wt. %, from about 11 wt. % toabout 19 wt. %, from about 11 wt. % to about 18 wt. %, from about 11 wt.% to about 17 wt. %, from about 11 wt. % to about 16 wt. %, from about11 wt. % to about 15 wt. %, from about 12 wt. % to about 25 wt. %, fromabout 12 wt. % to about 23 wt. %, from about 12 wt. % to about 21 wt. %,from about 12 wt. % to about 20 wt. %, from about 12 wt. % to about 19wt. %, from about 12 wt. % to about 18 wt. %, from about 12 wt. % toabout 17 wt. %, from about 12 wt. % to about 16 wt. %, from about 12 wt.% to about 15 wt. %, from about 13 wt. % to about 25 wt. %, from about13 wt. % to about 23 wt. %, from about 13 wt. % to about 21 wt. %, fromabout 13 wt. % to about 20 wt. %, from about 13 wt. % to about 19 wt. %,from about 13 wt. % to about 18 wt. %, from about 13 wt. % to about 17wt. %, from about 13 wt. % to about 16 wt. %, from about 13 wt. % toabout 15 wt. %, from about 14 wt. % to about 25 wt. %, from about 14 wt.% to about 23 wt. %, from about 14 wt. % to about 21 wt. %, from about14 wt. % to about 20 wt. %, from about 14 wt. % to about 19 wt. %, fromabout 14 wt. % to about 18 wt. %, from about 14 wt. % to about 17 wt. %,from about 14 wt. % to about 16 wt. %, or from about 14 wt. % to about15 wt. % all based on the total weight of the wet starch precursor. Itwill be understood that when preparing the wet starch, the moisturecontents described herein include ambient moisture as well as wateradded.

While not wishing to be bound by any particular theory, it is believedthat a lower moisture content leads to greater friction in the extruder.In some embodiments, the wet starch can be prepared to have a moisturecontent that allows for sufficient mechanical energy input when the wetstarch is fed through the extruder, such that friction prevents the wetstarch from moving through the extruder too easily. The increasedfriction can increase the disruption of hydrogen bonding in the starch.

Any suitable weak acid that substantially avoids chelating calcium ionsmay be mixed into the wet starch. Without wishing to be bound by anyparticular theory, chelation includes the weak acid, for example,forming a coordination complex with calcium or otherwise interferingwith the formation of gypsum crystals within the gypsum slurry. Suchinterference may be the reduction in number of gypsum crystals formed,retardation (decreased rate) of formation of the crystals, decreasinginteractions among the gypsum crystals, etc. The term “substantially”with respect to not chelating calcium ions generally means that at least90% (e.g., at least 92%, at least 95%, at least 96%, at least 97%, atleast 98%, or at least 99%) of the available calcium ions are notchelated to the acid.

Weak acids in accordance with embodiments of the invention can bedefined as those having a pKa value from about 1 to about 6, e.g., fromabout 1 to about 5, from about 1 to 4, from about 1 to 3, from about 1to 2, from about 1.2 to about 6, from about 1.2 to about 5, from about1.2 to about 4, from about 1.2 to about 3, from about 1.2 to about 2,from about 2 to about 6, from about 2 to about 5, from about 2 to about4, from about 2 to about 3, from about 3 to about 6, from about 3 toabout 5, from about 3 to about 4, from about 4 to about 6, or from about4 to about 5. As is understood in the art, the pKa value is a measure ofthe strength of an acid; the lower the pKa value, the stronger the acid.

Weak acids that substantially avoid chelating calcium ions arecharacterized, for example, by a lack of multi-binding sites, such asmultiple carboxyl functional groups (COO)—), which tend to bind calciumions. In some embodiments, the weak acid has a minimal amount ofmulti-binding sites, such as multi-COO— groups, or is substantially freeof multi-binding sites, such as multi-COO— groups, such that, forexample, chelation is minimal (i.e., substantially avoided) or gypsumcrystal formation is not substantially impacted relative to the crystalformation in the absence of the weak acid. In some embodiments, forexample, aluminum sulfate (alum) is an appropriate weak acid to use inpreparing the wet starch since it substantially avoids chelating calciumions. Alum does not have multi-binding sites.

In some embodiments, alum is added into the wet starch precursor in anysuitable form, such as in liquid containing alum of desired solidscontent. For example, the liquid alum can be included in an aqueoussolution where the alum is present in any suitable amount. Other weakacids can be added similarly.

The wet starch can be mixed to include any suitable amount of a weakacid that substantially avoids chelating calcium ions, such that thepregelatinized, partially hydrolyzed starch is prepared with desiredviscosity and low water demand and is not over hydrolyzed into sugar.For example, in some embodiments, such weak acid is included in anamount of from about 0.5 wt. % to about 5 wt. % based on the weight ofthe starch, such as from about 0.5 wt. % to about 4.5 wt. %, e.g., fromabout 0.5 wt. % to about 4 wt. %, from about 0.5 wt. % to about 3.5 wt.%, from about 0.5 wt. % to about 3 wt. %, from about 1 wt. % to about 5wt. %, from about 1 wt. % to about 4.5 wt. %, from about 1 wt. % toabout 4 wt. %, from about 1 wt. % to about 3.5 wt. %, from about 1 wt. %to about 3 wt. %, from about 1.5 wt. % to about 5 wt. %, from about 1.5wt. % to about 4.5 wt. %, from about 1.5 wt. % to about 4 wt. %, fromabout 1.5 wt. % to about 3.5 wt. %, from about 1.5 wt. % to about 3 wt.%, from about 2 wt. % to about 5 wt. %, from about 2 wt. % to about 4.5wt. %, from about 2 wt. % to about 4 wt. %, from about 2 wt. % to about3.5 wt. %, from about 2 wt. % to about 3 wt. %, from about 2.5 wt. % toabout 5 wt. %, from about 2.5 wt. % to about 4.5 wt. %, from about 2.5wt. % to about 4 wt. %, from about 2.5 wt. % to about 3.5 wt. %, or fromabout 2.5 wt. % to about 3 wt. %. It will be understood that theseamounts encompass the weak acid component, and, when the weak acid is ina solution, excludes the water or other components of the solution.

The wet starch precursor can be prepared to optionally further comprisesecondary acids that can chelate calcium ion, such as tartaric acid.Thus, in some embodiments, a secondary acid, such as tartaric acid, canbe combined with any suitable weak acid that does not chelate calciumions. Tartaric acid is known to retard gypsum crystallization. However,in combination with the non-chelating weak acid, tartaric acid avoidssubstantial retarding of gypsum crystallization, such that thehydrolysis reaction via acid-modification is optimized. Besides tartaricacid, other secondary acids, such as succinic acid or malic acid, may bebeneficial so long as they do not surpass the accelerating effect ofalum. In some embodiments, the wet starch precursor includes both alumand tartaric acid.

If included, secondary acids (e.g., tartaric acid) can be present in anysuitable amount. For example, tartaric acid can be present in an amountof from about 0.1 wt. % to about 0.6 wt. % based on the weight of thestarch, e.g., from about 0.1 wt. % to about 0.4 wt. %, from about 0.2wt. % to about 0.3 wt. %.

In some embodiments, oil can optionally be added to the wet starch toimprove the conveyability of starch inside the extruder. Possible oilsinclude canola oil, vegetable oil, corn oil, soybean oil, or anycombination thereof, in some embodiments. For example, in someembodiments, canola oil or one of the aforementioned substitutes canoptionally be added in an amount of from about 0 wt. % to about 0.25 wt.% by weight of the starch, e.g., from about 0.1 wt. % to about 0.2 wt.%, from about 0.1 wt. % to about 0.15 wt. %, from about 0.15 wt. % toabout 0.25 wt. %, from about 0.15 wt. % to about 0.2 wt. %, or fromabout 0.2 wt % to about 0.25 wt. %.

In accordance with some embodiments, the wet starch precursor isprepared by mixing water, non-pregelatinized starch, and a small amountof a strong acid. In some embodiments, the strong acid has a pKa ofabout −1.7 or less. Any such strong acid can be used and, in someembodiments, the strong acid comprises sulfuric acid, nitric acid,hydrochloric acid, or any combination thereof. Sulfuric acid, alone orin combination with other acids, is preferred in some embodimentsbecause sulfate ion can accelerate gypsum crystallization in gypsumboard embodiments.

The amount of strong acid is relatively small, such as about 0.05 wt. %or less by weight of the starch, e.g., about 0.045 wt. % or less, about0.04 wt. % or less, about 0.035 wt. % or less, about 0.03 wt. % or less,about 0.025 wt. % or less, about 0.02 wt. % or less, about 0.015 wt. %or less, about 0.01 wt. % or less, about 0.005 wt. % or less, about0.001 wt. % or less, about 0.0005 wt. % or less, such as from about0.0001 wt. % to about 0.05 wt. %, from about 0.0001 wt. % to about 0.045wt. %, from about 0.0001 wt. % to about 0.04 wt. %, from about 0.0001wt. % to about 0.035 wt. %, from about 0.0001 wt. % to about 0.03 wt. %,from about 0.0001 wt. % to about 0.025 wt. %, from about from about0.0001 wt. % to about 0.02 wt. %, from about 0.0001 wt. % to about 0.015wt. %, from about 0.0001 wt. % to about 0.01 wt. %, from about 0.0001wt. % to about 0.005 wt. %, from about 0.0001 wt. % to about 0.001 wt.%, from about 0.0001 wt. % to about 0.0005 wt. % by weight of thestarch. It will be understood that these amounts encompass the strongacid component, and, when the strong acid is in a solution, excludes thewater or other components of the solution. For example, conventionalstrong acid-modification uses 2% sulfuric acid solution, with starchsolid of ˜35% (2 g sulfuric acid for 35 g starch). The percent is basedon pure sulfuric acid components. It is calculated as the weight ofsulfuric acid component divided by the weight of the wet starch. Forexample, if the sulfuric acid is 50% pure (which means that half theweight of the solution is pure sulfuric acid), then the weight of thesulfuric acid solution is doubled. To illustrate, for 100 g starch, 0.1g pure sulfuric acid is added to achieve 0.1 wt. %. If the concentrationof sulfuric solution is 50%, 0.2 g of the 50% sulfuric acid solution isadded to achieve 0.1 wt. %.

It will be understood that there are different grades of acids (>95%,98%, 99.99%). These differences are encompassed by the term “about” inrelation to the amount of strong acid in the starch precursor. One ofordinary skill in the art will readily be able to determine the wt. %described herein to include the different grades. The amounts of strongacid used in accordance with some embodiments of the invention areconsiderably smaller than what were included in conventional systemswhich used, e.g., at least about 2 g of sulfuric acid for 35 g ofstarch. In some embodiments, the strong acid in small amounts asdescribed above can be used in combination with a weak acid that doesnot chelate calcium ions, such as alum, as described herein.

Embodiments of the invention provide feeding the wet starch precursorthrough an extruder, such that the wet starch precursor ispregelatinized and acid-modified in a single step in the extruder. Itwill be appreciated that an extruder is a machine generally used to meltand process polymers into a desired shape by melting the polymer andpumping it through a die. The extruder can also mix the polymer withother ingredients, such as color, reinforcing fibers, mineral fillers,etc. The purpose of the extruder is to disperse and distribute all ofthe ingredients fed into it and to melt the ingredients with a constanttemperature and pressure.

Configurations and arrangements for extruders are known in the art. Ingeneral, an extruder comprises a feed hopper to deliver the feedmaterial, a preconditioner comprising heat jackets for conditioningpolymer with plasticizer (e.g., water), an extruder modular headcomprising heating zones, and a die assembly. Extruders generallyinclude a feed auger, a knife, and screw(s). The feed auger is presentto help convey the wet starch precursor into the extruder. The knife ispresent to cut the string-like pregelatinized, partially hydrolyzedstarch into small pellets, such that they can be ground. The screw(s)help mix the wet starch precursor, convey the wet starch precursorthrough the extruder, and provide mechanical shearing. An extruder canbe of the single-screw or twin-screw varieties as will be understood byone of ordinary skill in the art. See, e.g., Leszek Moscicki,Extrusion-Cooking Techniques, WILEY-VCH Verlag & Co. KGaA, 2011.

In single-screw extruders, the screw generally comprises a feed sectionwith deep channels for transporting the solids from the throat of thefeeder and compressing them, a compression section at which point thescrew's channels become progressively less deep and the polymer ismelted, and a metering section with shallow channels that conveys themelted polymer to the die. Some screws are designed to include mixingdevices (e.g., pins extending from the screw).

Twin-screw extruders generally have two screws that rotate either in thesame direction (i.e., co-rotating) or in opposite directions (i.e.,counter-rotating). The two screws may rotate with non-intermeshing orfully intermeshing flights. Whereas in the case of single-screwextruders, the material being fed fills the entire screw channel, in thecase of twin-screw extruders, only part of the screw channel is filled,such that downstream feedports or vents can be utilized for the additionof certain ingredients.

The die assembly generally comprises a plate, spacer, and die head. Whenextruding materials, the process can be either continuous, such that thematerial is extruded in an indefinite length, or semi-continuous, suchthat the material is extruded in pieces. Materials being extruded may behot or cold.

The invention provides a method of preparing pregelatinized, partiallyhydrolyzed starch in an extruder. Any suitable extruder can be used,such as a single-screw extruder (e.g., the Advantage 50 available fromAmerican Extrusion International, located in South Beloit, Ill.) or atwin-screw extruder (e.g., the Wenger TX52 available from Wenger locatedin Sabetha, Kans.).

As described herein, non-pregelatinized starch, an acid in the form of aweak acid that substantially avoids chelating calcium ions and/or astrong acid in a small amount, and water are mixed and fed into theextruder. In some embodiments, additional water may be added to theextruder. While in the extruder, a combination of heating elements andmechanical shearing melts and pregelatinizes the starch, the weak acidpartially hydrolyzes the starch to a desired molecular weight indicatedby viscosity as desirable as described herein. The conditions in theextruder, because of the mechanical energy, will also cause the starchmolecules to degrade, which partially produces the same effect ofacid-modification. It is believed that because the conditions in anextruder (e.g., high reaction temperature and high pressure) inaccordance with some embodiments facilitate this chemical reaction, aweak acid and/or low amounts of a strong acid can be used. The inventivemethod, thus, improves the efficiency of starch acid-modification.

The main screw(s) can be operated at any suitable speed, such thatdesired mixing and mechanical shearing are achieved. For example, insome embodiments the main screw can be operated at a speed of about 350RPM (± about 100 RPM). The feed auger can be operated at any suitablespeed to achieve desired feeding rate. For example, in some embodimentsthe feed auger can be operated at a speed of about 14 RPM (± about 5RPM).

The knife can be operated at any suitable speed. For example, in variousembodiments the knife can be operated at a speed of from about 400 RPMto about 1,000 RPM, e.g., from about 400 RPM to about 900 RPM, fromabout 400 RPM to about 800 RPM, from about 400 RPM to about 700 RPM,from about 400 RPM to about 600 RPM, from about 400 RPM to about 500RPM, from about 500 RPM to about 1,000 RPM, from about 500 RPM to about900 RPM, from about 500 RPM to about 800 RPM, from about 500 RPM toabout 700 RPM, from about 500 RPM to about 600 RPM, from about 600 RPMto about 1,000 RPM, from about 600 RPM to about 900 RPM, from about 600RPM to about 800 RPM, from about 600 RPM to about 700 RPM, from about700 RPM to about 1,000 RPM, from about 700 RPM to about 900 RPM, fromabout 700 RPM to about 800 RPM, from about 800 RPM to about 1,000 RPM,from about 800 RPM to about 900 RPM, or from about 900 RPM to about1,000 RPM.

The wet starch can be pregelatinized and acid-modified in an extruderhaving a die at any suitable temperature, such that the wet starchbecomes sufficiently pregelatinized without burning the materials. Forexample, the wet starch can be pregelatinized and acid-modified in anextruder having a die at a temperature of from about 150° C. (about 300°F.) to about 210° C. (about 410° F.), e.g., in various embodiments, fromabout 150° C. to about 205° C. (about 400° F.), from about 150° C. toabout 199° C. (about 390° F.), from about 150° C. to about 193° C.(about 380° F.), from about 150° C. to about 188° C. (about 370° F.),from about 150° C. to about 182° C.: (about 360° F.), from about 154° C.(about 310° F.) to about 210° C., from about 154° C. to about 205° C.(about 400° F.), from about 154° C. to about 199° C., from about 154° C.to about 193° C., from about 154° C. to about 188° C., from about 154°C. to about 182° C., from about 160° C. (about 320° F.) to about 210°C., from about 160° C. to about 205° C. (about 400° F.), from about 160°C. to about 199° C., from about 160° C. to about 193° C., from about160° C. to about 188° C., from about 160° C. to about 182° C., fromabout 166° C. (about 330° F.) to about 210° C., from about 166° (toabout 205° C., from about 166° (to about 199° C., from about 166° C. toabout 193° C., from about 166° (C to about 188° (C, from about 166° C.to about 182° C., from about 171° C. (about 340° F.) to about 210° C.,from about 171° C. to about 205° C., from about 171° C. to about 199°C., from about 171° C. to about 193° C., from about 171° C. to about188° C., from about 171° C. to about 182° C., from about 177° C. (about350° F.) to about 210° C., from about 177° C. to about 205° C., fromabout 177° C. to about 199° C., from about 177° C. to about 193θ(C, fromabout 177° C. to about 188° C., or from about 177° C. to about 182° C.While the die of the extruder can be any sufficient temperature asdescribed herein, the die temperature generally exceeds the meltingtemperature of the starch crystals.

The degree of gelatinization can be any suitable amount, such as atleast about 70% or more. e.g., at least about 75%, at least about 80%,at least about 85%, at least about 90%, at least about 95%, at leastabout 97%, at least about 99%, or full (100%) gelatinization. In thecase of making wallboard as described below, starch with such lowerdegrees of gelatinization can be added to stucco slurry. e.g., withadditional gelatinization (for example, to 100%) taking place in thekiln.

The pressure in the extruder can be at any suitable level, such thatappropriate conditions for pregelatinization and acid-modification areachieved. Pressure inside the extruder is determined by the raw materialbeing extruded, moisture content, die temperature, and screw speed,which will be recognized by one of ordinary skill in the art. Forexample, the pressure in the extruder can be at least about 2,000 psi(about 13,800 kPa), such as at least about 2,250 psi (about 15,500 kPa),at least about 2,500 psi (about 17,200 kPa), at least about 2,750 psi(about 19,000 kPa), at least about 3,000 psi (about 20,650 kPa), atleast about 3,500 psi (about 24,100 kPa), at least about 4,000 psi(about 27,600 kPa), or at least about 4,500 psi (about 31,000 kPa). Insome embodiments, the pressure can be from about 2,000 psi to about5,000 psi (34,500 kPa), e.g., from about 2,000 psi to about 4,500 psi,from about 2,000 psi to about 4,000 psi, from about 2,000 psi to about3,500 psi, from about 2,000 psi to about 3,000 psi, from about 2,000 psito about 2,500 psi, from about 2,500 psi to about 5,000 psi, from about2,500 psi to about 4,500 psi, from about 2,500 psi to about 4,000 psi,from about 2,500 psi to about 3,500 psi, from about 2,500 psi to about3,000 psi, from about 3,000 psi to about 5,000 psi, from about 3,000 psito about 4,500 psi, from about 3,000 psi to about 4.000 psi, from about3,000 psi to about 3,500 psi, from about 3,500 psi to about 5,000 psi,from about 4,000 psi to about 5,000 psi, from about 4,000 psi to about4,500 psi, or from about 4,500 psi to about 5,000 psi.

Surprisingly and unexpectedly, it has been found that the inventivemethod of preparing pregelatinized, partially hydrolyzed starch in asingle step in an extruder is considerably faster than pregelatinizingand acid-modifying starch in two steps in series. Significantly greateramounts of pregelatinized, partially hydrolyzed starch can be preparedwith the inventive method than starch prepared with any other method.The higher production amount and faster output rate are because of highreaction rate at high temperature and/or high pressure. In someembodiments, pregelatinization and acid-modification occur in less thanabout 5 minutes, such as less than about 4 minutes. e.g., less thanabout 3 minutes, less than about 2 minutes, less than about 90 seconds,less than about 75 seconds, less than about 1 minute, less than about 45seconds, less than about 30 seconds, less than about 25 seconds, lessthan about 20 seconds, less than about 15 seconds, or less than about 10seconds. In addition, in some embodiments, the pregelatinization andacid-modification occur at a rate in the extruder bound by any two ofthe foregoing points. For example, the pregelatinization andacid-modification rate can be between about 10 seconds and 5 minutes,e.g., between about 10 seconds and about 4 minutes, between about 10seconds and about 3 minutes, between about 10 seconds and about 2minutes, between about 10 seconds and about 90 seconds, between about 10seconds and about 75 seconds, between about 10 seconds and about 1minute, between about 10 seconds and about 45 seconds, between about 10seconds and about 30 seconds, between about 10 seconds and about 25seconds, between about 10 seconds and about 20 seconds, or between about10 seconds and about 15 seconds.

The inventive method of preparing pregelatinized, partially hydrolyzedstarch can be a continuous process occurring at any sufficient rate. Insome embodiments, starch is pregelatinized and acid-modified at aproduction output rate in an extruder of at least about 100 kg/hr, suchas at least about 150 kg/hr, at least about 200 kg/hr, at least about250 kg/hr, at least about 300 kg/hr, at least about 350 kg/hr, at leastabout 400 kg/hr, at least about 450 kg/hr, 500 kg/hr, at least about 550kg/hr, e.g., at least about 600 kg/hr, at least about 650 kg/hr, atleast about 700 kg/hr, at least about 750 kg/hr, at least about 800kg/hr, at least about 850 kg/hr, at least about 900 kg/hr, at leastabout 950 kg/hr, at least about 1,000 kg/hr, at least about 1,050 kg/hr,at least about 1,100 kg/hr, at least about 1,150 kg/hr, at least about1,200 kg/hr, at least about 1,250 kg/hr, at least about 1,300 kg/hr, atleast about 1,350 kg/hr, at least about 1,400 kg/hr, at least about1,450 kg/hr, or at least about 1,500 kg/hr. In addition, in someembodiments, the production output rate in an extruder can be bound byany two of the foregoing points. For example, the production output ratecan be between about 100 kg/hr and about 1,500 kg/hr (e.g., betweenabout 100 kg/hr and about 1,500 kg/hr, between about 100 kg/hr and 1,000kg/hr, between about 250 kg/hr and about 1,500 kg/hr, between about 250kg/hr and about 1,000 kg/hr, between about 600 kg/hr and about 1,250kg/hr, between about 650 kg/hr and about 1,200 kg/hr, between about 700kg/hr and about 1,100 kg/hr, between about 750 kg/hr and about 1,000kg/hr, etc.).

It has been found by the inventors that in some embodiments theconditions in an extruder (e.g., high temperature and high pressure) areparticularly conducive to efficiently and sufficiently pregelatinizingand acid-modifying starch in a single step. When the extruder mixes thewet starch, it creates very high friction, thereby generating heat. Theshear force is created by the screw in the extruder because the spacebetween the screw and chamber in the extruder is very small. Specificmechanical energy (SME) describes mechanical energy of an object perunit of mass. SME will depend on the moisture content. Higher moisturecontent (e.g., for purposes of fluidity) will result in low viscosityand low friction and, thus, a smaller SME. If more moisture is present,a smaller SME will result because of low viscosity and low friction. Themoisture contents in the wet starch precursor of the invention asdescribed herein provide effective SME.

In the extruder, because of the conditions provided by embodiments ofthe invention as described herein, the starch is pregelatinized highlyefficiently. While not wishing to be bound by any particular theory, itis believed that the good mixing in the extruder in accordance with someembodiments of the invention requires less water for reaction in anextruder. Very low moisture content facilitates a high concentration ofreactant, which can accelerate the chemical reaction rate. The hightemperature of the extruder also significantly accelerates the reactionrate. When the starch leaves the extruder, the reaction has occurred,such that it is pregelatinized and partially hydrolyzed.

In conventional acid-modification, starch is added into a strong acidsolution. This conventional method uses significantly more water andacid than the surprising and unexpected method of simultaneouslypregelatinizing and acid-modifying starch in one step in an extruder asdescribed herein rather than in series. Conventional acid-modificationtakes several hours. After the reaction has taken place, the acid needsto be neutralized, purified, and washed away. The neutralization andpurification steps are time consuming and costly.

Until the inventors' surprising and unexpected discovery, it was thoughtundesirable to use a weak acid that substantially avoids chelatingcalcium ions or a strong acid in a small amount in conventionalacid-modification. This is because, in the conventional method, theweaker the acid is or the smaller the amount of a strong acid is, thelonger acid-modification takes. Thus, a strong acid (e.g., having a pKaof below about −1.7) in high amounts was desired in conventionalacid-modification. Surprisingly and unexpectedly, when pregelatinized,partially hydrolyzed starch is prepared in an extruder according toembodiments of the invention using a weak acid or a strong acid in asmall amount as described herein, there is no need for neutralizationand purification steps, due to the mild acidic condition and lessinterference with gypsum crystallization, respectively. In someembodiments, there can still be acid present in the pregelatinized,partially hydrolyzed starch.

Properties of Starch and Advantages of Using the Starch in Gypsum Board

The starch prepared in an extruder in accordance with embodiments of theinvention can be any pregelatinized, partially hydrolyzed starch. Insome embodiments, the starch can be prepared to have various propertiesas desired (e.g., mid-range viscosity, cold water solubility, cold waterviscosity, etc.) as described herein.

Pregelatinized, partially hydrolyzed starches prepared in an extruder inaccordance with embodiments of the invention can be suitable for use ingypsum board. For application in gypsum board, for instance,pregelatinization and acid-modification are beneficial, e.g., forstrength purposes by achieving a desired viscosity (and, hence,molecular weight range) in accordance with embodiments of the inventionas described herein. In the method of making wallboard discussed herein,the starch that is introduced into the stucco slurry can be at leastabout 70% gelatinized, e.g., at least about 75% gelatinized, at leastabout 80% gelatinized, at least about 85% gelatinized, at least about90% gelatinized, at least about 95% gelatinized, at least about 97%gelatinized, or 100% gelatinized (i.e., fully gelatinized).

Furthermore, feeding a wet starch comprising a weak acid thatsubstantially avoids chelating calcium ions as described herein into anextruder, in accordance with embodiments of the invention, hydrolyzesthe starch, such that a desired viscosity is achieved, thus indicating adesired molecular weight range is achieved. Viscosity thereby indicatesthe molecular weight of the pregelatinized, partially hydrolyzed starch,as will be appreciated by one of ordinary skill in the art.

In some embodiments, pregelatinized, partially hydrolyzed starchprepared in accordance with embodiments of the invention can be preparedto have any suitable viscosity. In some embodiments, the viscosity ischaracterized as having a “mid-range” viscosity (i.e., having aviscosity from about 20 centipoise to about 700 centipoise) when thepregelatinized, partially hydrolyzed starch is subjected to conditionsaccording to the VMA method with the pregelatinized, partiallyhydrolyzed starch in water in an amount of 15% by weight of the totalweight of the pregelatinized, partially hydrolyzed starch and water.Thus, the VMA method is used to determine whether the pregelatinized,partially hydrolyzed starch exhibits the mid-range viscositycharacteristic when subjected to the conditions of the VMA method. Thisdoes not mean that the pregelatinized, partially hydrolyzed starch mustbe added to the gypsum slurry under these conditions. Rather, whenadding the pregelatinized, partially hydrolyzed starch to slurry, it canbe in wet (in various concentrations of starch in the water) or dryforms, and it need not be fully gelatinized as described herein orotherwise under the conditions set forth in the VMA method.

In some embodiments, the mid-range viscosity of the pregelatinizedstarch can be from about 20 centipoise to about 700 centipoise, such asfrom about 20 centipoise to about 500 centipoise, from about 30centipoise to about 200 centipoise, or from about 100 centipoise toabout 700 centipoise. In embodiments of the invention, the viscosity ofthe pregelatinized starch when tested under the VMA method can be, e.g.,as listed in Tables 1A, 1B and 1C below. In the tables, an “X”represents the range “from about [corresponding value in top row] toabout [corresponding value in left-most column].” The indicated valuesrepresent viscosity of the pregelatinized starch in centipoise. For easeof presentation, it will be understood that each value represents“about” that value. For example, the first “X” in Table 1A is the range“about 20 centipoise to about 25 centipoise.”

TABLE 1A Starting Point for Viscosity Range (centipoise) 20 25 30 35 4045 50 55 60 65 70 75 End Point 25 X for 30 X X Viscosity 35 X X X Range40 X X X X (centipoise) 45 X X X X X 50 X X X X X X 55 X X X X X X X 60X X X X X X X X 65 X X X X X X X X X 70 X X X X X X X X X X 75 X X X X XX X X X X X 100 X X X X X X X X X X X X 125 X X X X X X X X X X X X 150X X X X X X X X X X X X 175 X X X X X X X X X X X X 200 X X X X X X X XX X X X 225 X X X X X X X X X X X X 250 X X X X X X X X X X X X 275 X XX X X X X X X X X X 300 X X X X X X X X X X X X 325 X X X X X X X X X XX X 350 X X X X X X X X X X X X 375 X X X X X X X X X X X X 400 X X X XX X X X X X X X 425 X X X X X X X X X X X X 450 X X X X X X X X X X X X475 X X X X X X X X X X X X 500 X X X X X X X X X X X X 525 X X X X X XX X X X X X 550 X X X X X X X X X X X X 575 X X X X X X X X X X X X 600X X X X X X X X X X X X 625 X X X X X X X X X X X X 650 X X X X X X X XX X X X 675 X X X X X X X X X X X X 700 X X X X X X X X X X X X

TABLE 1B Starting Point for Viscosity Range (centipoise) 100 125 150 175200 225 250 275 300 325 350 375 End Point 125 X for 150 X X Viscosity175 X X X Range 200 X X X X (centipoise) 225 X X X X X 250 X X X X X X275 X X X X X X X 300 X X X X X X X X 325 X X X X X X X X X 350 X X X XX X X X X X 375 X X X X X X X X X X X 400 X X X X X X X X X X X X 425 XX X X X X X X X X X X 450 X X X X X X X X X X X X 475 X X X X X X X X XX X X 500 X X X X X X X X X X X X 525 X X X X X X X X X X X X 550 X X XX X X X X X X X X 575 X X X X X X X X X X X X 600 X X X X X X X X X X XX 625 X X X X X X X X X X X X 650 X X X X X X X X X X X X 675 X X X X XX X X X X X X 700 X X X X X X X X X X X X

TABLE 1C Starting Point for Viscosity Range (centipoise) 400 425 450 475500 525 550 575 600 625 650 675 End Point 425 X for 450 X X Viscosity475 X X X Range 500 X X X X (centipoise) 525 X X X X X 550 X X X X X X575 X X X X X X X 600 X X X X X X X X 625 X X X X X X X X X 650 X X X XX X X X X X 675 X X X X X X X X X X X 700 X X X X X X X X X X X X

Thus, the viscosity of the pregelatinized, partially hydrolyzed starchprepared in accordance with embodiments of the invention can have arange between and including any of the aforementioned endpoints setforth in Tables 1A, 1B or 1C. Alternatively, in some embodiments, thepregelatinized, partially hydrolyzed starch has a viscosity (10% solids,93° C.) of from about 5 Brabender Units (BU) to about 33 BU, measuredaccording to the Brabender method described herein, e.g., from about 10BU to about 30 BU, from about 12 BU to about 25 BU, or from about 15 BUto about 20 BU.

In some embodiments, pregelatinized, partially hydrolyzed starchesprepared in accordance with embodiments of the invention can providesignificant benefits to the strength of the product (e.g., wallboard) towhich they are applied. Since starch contains glucose monomerscontaining three hydroxyl groups, starch provides many sites forhydrogen bonding to gypsum crystals. While not wishing to be bound byany particular theory, it is believed that the molecular size ofpregelatinized, partially hydrolyzed starch prepared in accordance withembodiments of the invention allows for optimal mobility of starchmolecules to align starch molecules with the gypsum crystals tofacilitate good binding of starch to gypsum crystals to strengthen theresulting crystalline gypsum matrix. e.g., via hydrogen bonding.

Conventional pregelatinized starches prepared according to anothermethod than that which is described herein, e.g., having viscositiesoutside the mid-range, which would have either longer chain lengths andhigher molecular weight (viscosity that is too high) and shorter chainlengths and lower molecular weights (viscosity that is too low),respectively, do not provide the same combination of benefits. It isalso believed that, with respect to starch efficiency, when the starchmolecules sufficiently bind to the gypsum crystals, additional starchdoes not add significant benefit because the crystals are already boundsuch that there is no further gypsum crystal sites for which the starchto adhere or bind. Accordingly, because of the optimal binding betweengypsum crystals and the molecules of pregelatinized, partiallyhydrolyzed starch prepared in accordance with embodiments of theinvention, the strength of the crystalline gypsum matrix is enhanced,and less starch is required to promote that strength compared withconventional starches. The inventors have found dissolved starchmolecules with, for example, mid-range viscosity (representing mid rangemolecular weight of starch) allows for optimal mobility of starchmolecules to align starch molecules with gypsum crystals to facilitategood starch and gypsum hydrogen-bonding and core strength in someembodiments.

Pregelatinized, partially hydrolyzed starch prepared in accordance withsome embodiments of the invention also provides advantages with respectto water demand, in some embodiments. Adding conventional pregelatinizedstarch to gypsum slurry requires that additional water be added to thegypsum slurry in order to maintain a desired degree of slurry fluidity.This is because conventional pregelatinized starch increases theviscosity and reduces the fluidity of the gypsum slurry. Thus, the useof pregelatinized starch in conventional systems has resulted in anincrease in water demand such that even more excess water would berequired in the gypsum slurry.

Surprisingly and unexpectedly, pregelatinized, partially hydrolyzedstarch prepared in accordance with embodiments of the invention,particularly with the desired mid-range viscosity, demands less water sothat the effect on water demand in the gypsum slurry is reduced,especially in comparison to conventional starches. Furthermore, becauseof the efficiency of the pregelatinized, partially hydrolyzed starchprepared in accordance with embodiments of the invention, such that lessstarch can be used, the positive impact on water demand can be even moresignificant in accordance with some embodiments of the invention. Thislower water demand provides considerable efficiencies duringmanufacture. For example, excess water requires energy input for drying.The speed of the line must be slowed to accommodate the drying. Thus, byreducing the water load in the gypsum slurry, less energy resources andcost can be seen, as well as faster production rates. In someembodiments, the increase in water demand in a gypsum slurry is lessthan the increase in water demand required by other starches such aspregelatinized starches having viscosity above 700 centipoise (e.g.,about 773 centipoise), e.g., prepared by a different method.

Any suitable non-pregelatinized starch can be selected in preparing apregelatinized, partially hydrolyzed starch so long as it is sufficientto be pregelatinized and acid-modified in an extruder. As used herein,“starch” refers to a composition that includes a starch component. Assuch, the starch can be 100% pure starch or may have other componentssuch as those commonly found in flours such as protein and fiber, solong as the starch component makes up at least about 75% by weight ofthe starch composition. The starch can be in the form of a flour (e.g.,corn flour) containing starch, such as flour having at least about 75%starch by weight of the flour, e.g., at least about 80%, at least about85%, at least about 90%, at least about 95%, etc.). By way of example,and not in any limitation, the starch can be in the form of a corn flourcontaining starch.

In some embodiments, the pregelatinized, partially hydrolyzed starchprepared in accordance with embodiments of the invention can be preparedto have desired cold water solubility. Conventional pregelatinizationtechniques involve making starch cold water soluble and generallyrequire cooking starch in an excess amount of water. However, theseconventional techniques are not efficient. Extrusion, in accordance withembodiments of the invention, which allows for a combination of heatingand mechanical shearing, is surprisingly and unexpectedly an energyefficient method that can be used to produce pregelatinized, partiallyhydrolyzed starch in a one step process having a low moisture contentwith cold water solubility. Cold water solubility is defined as havingany amount of solubility in water at room temperature (about 25° C.). Itwas discovered that starches exhibiting solubility in cold water canprovide significant benefits to the strength of gypsum products (e.g.,wallboard). Cold water soluble starches of the present invention have acold water solubility greater than about 30% and, when added to a setgypsum core, can increase the strength of the gypsum core. Thesolubility of the pregelatinized starch in water is defined as theamount of starch that dissolves in room temperature water divided by thetotal amount of starch.

In some embodiments, the cold water solubility of the pregelatinized,partially hydrolyzed starch prepared in accordance with embodiments ofthe invention is from about 30% to about 100%. In other embodiments, thecold water solubility of the extruded pregelatinized, partiallyhydrolyzed starch is from about 50% to about 100%. In embodiments of theinvention, the cold water solubility of the extruded pregelatinized,partially hydrolyzed starch can be, e.g., as listed in Table 2. In thetable, an “X” represents the range “from about [corresponding value intop row] to about [corresponding value in left-most column].” Theindicated values represent the cold water solubility of a extrudedpregelatinized, partially hydrolyzed starch prepared in accordance withembodiments of the invention (Table 2). For ease of presentation, itwill be understood that each value represents “about” that value. Forexample, the first “X” in Table 2 is the range “from about 30% to about35%.” The ranges of the table are between and including the starting andendpoints.

TABLE 2 Starting Point for Cold Water Solubility Range (%) 30 35 40 4550 55 60 65 70 75 80 85 90 95 End Point 35 X for 40 X X Cold Water 45 XX X Solubility 50 X X X X Range (%) 55 X X X X X 60 X X X X X X 65 X X XX X X X 70 X X X X X X X X 75 X X X X X X X X X 80 X X X X X X X X X X85 X X X X X X X X X X X 90 X X X X X X X X X X X X 95 X X X X X X X X XX X X X 100 X X X X X X X X X X X X X X

While not wishing to be bound by any particular theory, it is believedthat a combination of mechanical and thermal energy during extrusion isresponsible for the cold water solubility of the pregelatinized,partially hydrolyzed starch prepared in accordance with embodiments ofthe invention. It is believed that when the starch undergoes extrusion,the hydrogen bonds between the starch molecules are broken. When theextruded starch is dissolved in water, the starch forms hydrogen bondswith the water molecules. After the pregelatinization process, theextruded pregelatinized, partially hydrolyzed starch molecules are freeto hydrogen-bond with the gypsum crystals, thus imparting higherstrength to the gypsum product. Accordingly, because starches exhibitingsolubility in cold water improves the strength of gypsum wallboard, lessstarch is required compared with conventional starches.

In some embodiments, the pregelatinized, partially hydrolyzed starch hasa cold water viscosity (10% solids, 25° C.) of from about 10 BU to about120 BU, measured according to the Brabender method described herein,e.g., from about 20 BU to about 110 BU, from about 30 BU to about 100BU, from about 40 BU to about 90) BU, from about 50 BU to about 80 BU,or from about 60 BU to about 70 BU.

Use of Starch Prepared According to the Method in Making Board

In some embodiments, a board (e.g., gypsum wallboard) can be made byforming a pregelatinized, partially hydrolyzed starch by) mixing atleast water, non-pregelatinized starch, and an acid to form a wet starchprecursor having a moisture content of from about 8 wt. % to about 25wt. %, the acid selected from: a weak acid that substantially avoidschelating calcium ions, a strong acid in an amount of about 0.01 wt. %or less by weight of the starch, or any combination thereof.

The wet starch precursor is then fed into an extruder in which thetemperature of the die of about 150° C. (about 300° F.) to about 210° C.(about 410° F.) where the wet starch is pregelatinized andacid-modified, such that it is at least partially hydrolyzed. Thepreglelatinized, partially hydrolyzed starch can then be mixed with atleast water and stucco to form a slurry, which can then be disposedbetween a first cover sheet and a second cover sheet to form a wetassembly. The wet assembly can then be cut into a board, which is thendried. Preferably, the set gypsum core of the board has a compressivestrength greater than a set gypsum core made with a starch preparedunder a different method.

The pregelatinized, partially hydrolyzed starch prepared in accordancewith embodiments of the invention surprisingly and unexpectedly can beincluded in the slurry in a relatively low amount (solids/solids basis)and still achieve significant strength enhancement in the board.Accordingly, the pregelatinized, partially hydrolyzed starch prepared inaccordance with embodiments of the invention can be included in thegypsum slurry in an amount that is from about 0.1% to about 10% byweight based on the weight of the stucco, e.g., from about 0.5% to about10%.

It has been found that increasing the amount of the pregelatinized,partially hydrolyzed starch prepared in accordance with embodiments ofthe invention in the slurry beyond these ranges does not improvestrength as efficiently since strength levels can somewhat plateau uponaddition of even more starch in some embodiments. However, higher starchquantities can be utilized if desired especially where the diminishingreturn on strength is accepted.

In embodiments of the invention, pregelatinized, partially hydrolyzedstarch can be added to the gypsum slurry in an amount, for example, aslisted in Tables 3A and 3B below. In the table, an “X” represents therange “from about [corresponding value in top row] to about[corresponding value in left-most column].” The indicated valuesrepresent the amount of starch as a percentage by weight of the stucco.For ease of presentation, it will be understood that each valuerepresents “about” that value. For example, the first “X” is the range“from about 0.1% of the starch by weight of the stucco, to about 0.25%of the starch by weight of the stucco.”

TABLE 3A 0.1 0.25 0.5 0.75 1.0 1.25 1.5 1.75 2.0 2.25 2.5 2.75 3.0 3.50.25 X 0.5 X X 0.75 X X X 1.0 X X X X 1.25 X X X X X 1.5 X X X X X X1.75 X X X X X X X 2.0 X X X X X X X X 2.25 X X X X X X X X X 2.5 X X XX X X X X X X 2.75 X X X X X X X X X X X 3.0 X X X X X X X X X X X X 3.5X X X X X X X X X X X X X 4.0 X X X X X X X X X X X X X X 4.5 X X X X XX X X X X X X X X 5.0 X X X X X X X X X X X X X X 5.5 X X X X X X X X XX X X X X 6.0 X X X X X X X X X X X X X X 6.5 X X X X X X X X X X X X XX 7.0 X X X X X X X X X X X X X X 7.5 X X X X X X X X X X X X X X 8.0 XX X X X X X X X X X X X X 8.5 X X X X X X X X X X X X X X 9.0 X X X X XX X X X X X X X X 9.5 X X X X X X X X X X X X X X 10.0 X X X X X X X X XX X X X X

TABLE 3B 4.0 4.5 5.0 5.5 6.0 6.5 7.0 7.5 8.0 8.5 9.0 9.5 4.5 X 5.0 X X5.5 X X X 6.0 X X X X 6.5 X X X X X 7.0 X X X X X X 7.5 X X X X X X X8.0 X X X X X X X X 8.5 X X X X X X X X X 9.0 X X X X X X X X X X 9.5 XX X X X X X X X X X 10.0 X X X X X X X X X X X X

Thus, the amount of the pregelatinized, partially hydrolyzed starchprepared in accordance with embodiments of the invention added to theslurry can have a range between and including any of the aforementionedendpoints set forth in Tables 3A or 3B.

Pregelatinized, partially hydrolyzed starch prepared in accordance withembodiments of the invention can be added to the slurry in combinationwith other starches, in some embodiments for various applications. Forexample, in the case of gypsum wallboard as described below,pregelatinized, partially hydrolyzed starch prepared in accordance withembodiments of the invention can be combined with other starches toenhance both core strength and paper-core bond, particularly if someincrease in water demand is accepted.

Thus, in some embodiments of the invention, gypsum slurry may includeone or more pregelatinized, partially hydrolyzed starch prepared inaccordance with embodiments of the invention, as well as one or moreother types of starches. Other starches can include, for example,pregelatinized starches having viscosity below 20 centipoise and/orabove 700 centipoise. One example is pregelatintzed corn starch (e.g.,having a viscosity over 700 centipoise such as about 773 centipoise).The other starches may also be in the form of, e.g., non-pregelatinizedstarches, such as acid-modified starches, as well as alkylated starches,e.g., ethylated starches, that are not gelatinized, etc. The combinationof starches may be pre-mixed (e.g., in a dry mix, optionally with othercomponents such as stucco, etc., or in a wet mix with other wetingredients) before addition to the gypsum slurry, or they can beincluded in the gypsum slurry one at a time, or any variation thereof.Any suitable proportion of pregelatinized, partially hydrolyzed starchprepared in accordance with embodiments of the invention and otherstarch may be included.

For example, the starch content of pregelatinized, partially hydrolyzedstarch prepared in accordance with embodiments of the invention as apercentage of total starch content to be added to gypsum slurry can be,e.g., at least about 10% by weight, such as at least about 20%, at leastabout 30%, at least about 40%, at least about 50%, at least about 60%,at least about 70%, at least about 80%, at least about 90%, at leastabout 95%, at least about 99%, at least about 100%, or any range inbetween). In some embodiments, the ratio of pregelatinized, partiallyhydrolyzed starch prepared in accordance with embodiments of theinvention to other starch can be about 25:75, about 30:70, about 35:65,about 50:50, about 65:35, about 70:30, about 75:25, etc.

In addition to the starch component, the slurry is formulated to includewater, stucco, foaming agent (sometimes referred to simply as “foam”),and other additives as desired, in some embodiments. Surprisingly andunexpectedly, in accordance with some embodiments, particularly thoseexhibiting a mid-range viscosity, it has been found that the amount ofwater needed to be added to maintain the slurry fluidity at the samelevel it would be without the pregelatinized, partially hydrolyzedstarch prepared in an extruder in accordance with embodiments of theinvention, is less than the increase in the amount of water needed whenusing a starch prepared according to a different method. The stucco canbe in the form of calcium sulfate alpha hemihydrate, calcium sulfatebeta hemihydrate, and/or calcium sulfate anhydrite. The stucco can befibrous or non-fibrous. Foaming agent can be included to form an airvoid distribution within the continuous crystalline matrix of setgypsum. In some embodiments, the foaming agent comprises a major weightportion of unstable component, and a minor weight portion of stablecomponent (e.g., where unstable and blend of stable/unstable arecombined). The weight ratio of unstable component to stable component iseffective to form an air void distribution within the set gypsum core.See, e.g., U.S. Pat. Nos. 5,643,510; 6,342,284; and 6,632,550.

It has been found that suitable void distribution and wall thickness(independently) can be effective to enhance strength, especially inlower density board (e.g., below about 35 pct). See, e.g., US2007/0048490 and US 2008/0090068. Evaporative water voids, generallyhaving voids of about 5 μm or less in diameter, also contribute to thetotal void distribution along with the aforementioned air (foam) voids.In some embodiments, the volume ratio of voids with a pore size greaterthan about 5 microns to the voids with a pore size of about 5 microns orless, is from about 0.5:1 to about 9:1, such as, for example, from about0.7:1 to about 9:1, from about 0.8:1 to about 9:1, from about 1.4:1 toabout 9:1, from about 1.8:1 to about 9:1, from about 2.3:1 to about 9:1,from about 0.7:1 to about 6:1, from about 1.4:1 to about 6:1, from about1.8:1 to about 6:1, from about 0.7:1 to about 4:1, from about 1.4:1 toabout 4:1, from about 1.8:1 to about 4:1, from about 0.5:1 to about2.3:1, from about 0.7:1 to about 2.3:1, from about 0.8:1 to about 2.3:1,from about 1.4:1 to about 2.3:1, from about 1.8:1 to about 2.3:1, etc.In some embodiments, the foaming agent is present in the slurry, e.g.,in an amount of less than about 0.5% by weight of the stucco such asabout 0.01% to about 0.5%, about 0.01% to about 0.4%, about 0.01% toabout 0.3%, about 0.01% to about 0.2%, about 0.01% to about 0.1%, about0.02% to about 0.4%, about 0.02% to about 0.3%, about 0.02% to about0.2%, etc., all by weight of the stucco.

Additives such as accelerator (e.g., wet gypsum accelerator, heatresistant accelerator, climate stabilized accelerator) and retarder arewell known and can be included, in some embodiments. See, e.g., U.S.Pat. Nos. 3,573,947 and 6,409,825. In some embodiments where acceleratorand/or retarder are included, the accelerator and/or retarder each canbe in the gypsum slurry in an amount on a solid basis of, e.g., fromabout 0% to about 10% by weight of the stucco (e.g., about 0.1% to about10%), such as, for example, from about 0% to about 5% by weight of thestucco (e.g., about 0.1% to about 5%). Other additives as desired may beincluded, e.g., to impart strength to enable lower weight product withsufficient strength, to avoid permanent deformation, to promote greenstrength, for example, as the product is setting on the conveyortraveling down a manufacturing line, to promote fire resistance, topromote water resistance, etc.

For example, the slurry can optionally include at least one dispersantto enhance fluidity in some embodiments. Like the pregelatinized,partially hydrolyzed starch prepared in accordance with embodiments ofthe invention and other ingredients, the dispersants may be included ina dry form with other dry ingredients and/or in a liquid form with otherliquid ingredients in the core slurry. Examples of dispersants includenaphthalenesulfonates, such as polynaphthalenesulfonic acid and itssalts (polynaphthalenesulfonates) and derivatives, which arecondensation products of naphthalenesulfonic acids and formaldehyde; aswell as polycarboxylate dispersants, such as polycarboxylic ethers, forexample, PCE211, PCE111, 1641, 1641F, or PCE 2641-Type Dispersants,e.g., MELFLUX 2641F, MELFLUX 2651F, MELFLUX 1641F, MELFLUX 2500Ldispersants (BASF), and COATEX Ethacryl M, available from Coatex, Inc.;and/or lignosulfonates or sulfonated lignin. Lignosulfonates arewater-soluble anionic polyelectrolyte polymers, byproducts from theproduction of wood pulp using sulfite pulping. One example of a ligninuseful in the practice of principles of embodiments of the presentinvention is Marasperse C-21 available from Reed Lignin Inc.

Lower molecular weight dispersants are generally preferred. Lowermolecular weight naphthalenesulfonate dispersants are favored becausethey trend to a lower water demand than the higher viscosity, highermolecular weight dispersants. Thus, molecular weights from about 3,000to about 10,000 (e.g., about 8,000 to about 10,000) are preferred. Asanother illustration, for PCE211 type dispersants, in some embodiments,the molecular weight can be from about 20,000 to about 60,000, whichexhibit less retardation than dispersants having molecular weight above60,000.

One example of a naphthalenesulfonate is DILOFLO, available from GEOSpecialty Chemicals. DILOFLO is a 45% naphthalenesulfonate solution inwater, although other aqueous solutions, for example, in the range ofabout 35% to about 55% by weight solids content, are also readilyavailable. Naphthalenesulfonates can be used in dry solid or powderform, such as LOMAR D, available from GEO Specialty Chemicals, forexample. Another exemplary naphthalenesulfonate is DAXAD, available fromHampshire Chemical Corp.

If included, the dispersant can be included in any suitable(solids/solids) amount, such as, for example, from about 0.1% to about5% by weight based on the weight of the stucco, e.g., from about 0.1% toabout 4%, from about 0.1% to about 3%, from about 0.2% to about 3%, fromabout 0.5% to about 3%, from about 0.5% to about 2.5%, from about 0.5%to about 2%, from about 0.5% to about 1.5%, etc.

In some embodiments, one or more phosphate-containing compounds can alsobe optionally included in the slurry, if desired. For example,phosphate-containing components useful in some embodiments includewater-soluble components and can be in the form of an ion, a salt, or anacid, namely, condensed phosphoric acids, each of which comprises two ormore phosphoric acid units: salts or ions of condensed phosphates, eachof which comprises two or more phosphate units; and monobasic salts ormonovalent ions of orthophosphates as well as water-soluble acyclicpolyphosphate salt. See, e.g., U.S. Pat. Nos. 6,342,284; 6,632,550;6,815,049; and 6,822,033.

Phosphate compositions if added in some embodiments can enhance greenstrength, resistance to permanent deformation (e.g., sag), dimensionalstability, etc. Trimetaphosphate compounds can be used, including, forexample, sodium trimetaphosphate, potassium trimetaphosphate, lithiumtrimetaphosphate, and ammonium trimetaphosphate. Sodium trimetaphosphate(STMP) is preferred, although other phosphates may be suitable,including for example sodium tetrametaphosphate, sodiumhexametaphosphate having from about 6 to about 27 repeating phosphateunits and having the molecular formula Na_(n+2)P_(n)O_(3n+1) whereinn=6-27, tetrapotassium pyrophosphate having the molecular formulaK₄P₂O₇, trisodium dipotassium tripolyphosphate having the molecularformula Na₃K₂P₃O₁₀, sodium tripolyphosphate having the molecular formulaNa₅P₃O₁₀, tetrasodium pyrophosphate having the molecular formulaNa₄P₂O₇, aluminum trimetaphosphate having the molecular formulaAl(PO₃)₃, sodium acid pyrophosphate having the molecular formulaNa₂H₂P₂O₇, ammonium polyphosphate having 1,000-3,000 repeating phosphateunits and having the molecular formula (NH₄)_(n+2)PnO_(3n+1) whereinn=1,000-3,000, or polyphosphoric acid having two or more repeatingphosphoric acid units and having the molecular formulaH_(n+2)P_(n)O_(3n+1) wherein n is two or more.

The phosphate can be included in some embodiments in a dry form or in aform in water (e.g., a phosphate solution from about 5% to about 20%,such as about a 10% solution). If included, the phosphate can be in anysuitable amount (solids/solids basis), such as from about 0.01% to about0.5% by weight based on the weight of stucco, e.g., from about 0.03% toabout 0.4%, from about 0.1% to about 0.3%, or from about 0.12% to about0.4% by weight based on the weight of stucco.

Suitable additives for fire-rated and/or water resistant product canalso optionally be included, including e.g., siloxanes (waterresistance); fiber; heat sink additives such as aluminum trihydrite(ATH), magnesium hydroxide or the like; and/or high expansion particles(e.g., expandable to about 300% or more of original volume when heatedfor about one hour at 1560° F.). See, e.g., co-pending, commonlyassigned U.S. application Ser. No. 13/400,010 (filed Feb. 17, 2012) fordescription of these and other ingredients. In some embodiments, highexpansion vermiculite is included, although other fire resistantmaterials can be included. The board of some fire-related productaccording to the invention can have a Thermal Insulation Index (TI) ofabout 17 minutes or greater, e.g., about 20 minutes or greater, about 30minutes or greater, about 45 minutes or greater, about 60 minutes orgreater, etc.; and/or a High Temperature Shrinkage (at temperatures ofabout 1560° F. (850° C.)) of less than about 10% in the x-y directionsand expansion in the z-direction of greater than about 20%. The fire orwater resistance additives can be included in any suitable amount asdesired depending, e.g., on fire rating, etc. For example, if included,the fire or water resistance additives can be in an amount from about0.5% to about 10% by weight of the stucco, such as from about 1% toabout 10%, about 1% to about 8%, about 2% to about 10%, about 2% toabout 8% by weight of the stucco, etc.

If included, in some embodiments, the siloxane preferably is added inthe form of an emulsion. The slurry is then shaped and dried underconditions which promote the polymerization of the siloxane to form ahighly cross-linked silicone resin. A catalyst which promotes thepolymerization of the siloxane to form a highly cross-linked siliconeresin can be added to the gypsum slurry. In some embodiments,solventless methyl hydrogen siloxane fluid sold under the name SILRES BS94 by Wacker-Chemie GmbH (Munich, Germany) can be used as the siloxane.This product is a siloxane fluid containing no water or solvents. It iscontemplated that about 0.3% to about 1.0% of the BS 94 siloxane may beused in some embodiments, based on the weight of the dry ingredients.For example, in some embodiments, it is preferred to use from about 0.4%to about 0.8% of the siloxane based on the dry stucco weight.

The slurry formulation can be made with any suitable water/stucco ratio,e.g., from about 0.4 to about 1.3. However, because the pregelatinized,partially hydrolyzed starches prepared in accordance with embodiments ofthe invention reduce the amount of water required to be added to theslurry to accommodate them, as compared with other starches (e.g.,conventional pregelatinized starch prepared according to a differentmethod), the slurry can be formulated with a water/stucco ratio inputthat is lower in some embodiments than what is conventional for otherstarch-containing gypsum slurries, especially at low weight/density. Forexample, in some embodiments, the water/stucco ratio can be from about0.4 to about 1.1, from about 0.4 to about 0.9, from about 0.4 to about0.85, from about 0.45 to about 0.85, from about 0.55 to about 0.85, fromabout 0.55 to about 0.8, from about 0.6 to about 0.9, from about 0.6 toabout 0.85, from about 0.6 to about 0.8, etc.

The cover sheets can be formed of any suitable material and basisweight. Advantageously, board core formed from slurry comprisingpregelatinized, partially hydrolyzed starch prepared in accordance withembodiments of the invention provides sufficient strength in board evenwith lower basis weight cover sheets such as, for example, less than 45lbs/MSF (e.g., about 33 lbs/MSF to 45 lbs/MSF) even for lower weightboard (e.g., having a density of about 35 pcf or below) in someembodiments. However, if desired, in some embodiments, heavier basisweights can be used, e.g., to further enhance nail pull resistance or toenhance handling, e.g., to facilitate desirable “feel” characteristicsfor end-users.

In some embodiments, to enhance strength (e.g., nail pull strength),especially for lower density board, one or both of the cover sheets canbe formed from paper and have a basis weight of, for example, at leastabout 45 lbs/MSF (e.g., from about 45 lbs/MSF to about 65 lbs/MSF, fromabout 45 lbs/MSF to about 60 lbs/MSF, from about 45 lbs/MSF to about 55lbs/MSF, from about 50 lbs/MSF to about 65 lbs/MSF, from about 50lbs/MSF to about 60 lbs/MSF, etc.). If desired, in some embodiments, onecover sheet (e.g., the “face” paper side when installed) can haveaforementioned higher basis weight, e.g., to enhance nail pullresistance and handling, while the other cover sheet (e.g., the “back”sheet when the board is installed) can have somewhat lower weight basisif desired (e.g., weight basis of less than about 45 lbs/MSF, e.g., fromabout 33 lbs/MSF to about 45 lbs/MSF or from about 33 lbs/MSF to about40 lbs/MSF).

Board weight is a function of thickness. Since boards are commonly madeat varying thicknesses, board density is used herein as a measure ofboard weight. The advantages of the pregelatinized, partially hydrolyzedstarch prepared in accordance with embodiments of the invention can beseen across various board densities, e.g., about 40 pcf or less, such asfrom about 20 pcf to about 40 pcf, from about 24 pcf to about 37 pcf,etc. However, preferred embodiments of the invention have particularutility at lower densities where the enhanced strength provided by thepregelatinized, partially hydrolyzed starch prepared in accordance withembodiments of the invention advantageously enables the use of lowerweight board with good strength and lower water demand than board madefrom other starches prepared according to a different method.

For example, in some embodiments, board density can be from about 20 pcfto about 35 pcf, e.g., from about 20 pcf to about 34 pcf, from about 20pcf to about 33 pcf, from about 20 pcf to about 32 pcf, from about 20pcf to about 31 pcf, from about 20 pcf to about 30 pcf, from about 20pcf to about 29 pcf, from about 21 pcf to about 35 pcf, from about 21pcf to about 34 pet, from about 21 pcf to about 33 pcf, from about 21pcf to about 32 pcf, from about 21 pcf to about 31 pcf, from about 21pcf to about 30 pcf, from about 21 pcf to about 29 pcf, from about 24pcf to about 35 pcf, from about 24 pcf to about 34 pcf, from about 24pcf to about 33 pcf, from about 24 pcf to about 32 pcf, from about 24pcf to about 31 pcf, from about 24 pcf to about 30 pcf, or from about 24pcf to about 29 pcf.

The pregelatinized, partially hydrolyzed starches prepared in accordancewith embodiments of the invention can be added to slurry to providestrength enhancement to product according to the invention, which can beespecially beneficial at lower weight/density. For example, in someembodiments, the board made according to embodiments of the inventionhas a compressive strength of at least about 400 psi (2,750 kPa) at adensity of 29 pcf as tested according to the method set forth in Example4. Advantageously, in various embodiments at various board densities asdescribed herein, the board produced by the inventive method can beprepared to have a compressive strength of at least about 400 psi, e.g.,at least about 450 psi (3,100 kPa), at least about 500 psi (3,450 kPa),at least about 550 psi (3,800 kPa), at least about 600 psi (4,100 kPa),at least about 650 psi (4,500 kPa), at least about 700 psi (4,800 kPa),at least about 750 psi (5,200 kPa), at least about 800 psi (5,500 kPa),at least about 850 psi (5,850 kPa), at least about 900 psi (6,200 kPa),at least about 950 psi (6,550 kPa), or at least about 1,000 psi (6,900kPa). In addition, in some embodiments, the compressive strength can bebound by any two of the foregoing points. For example, the compressivestrength can be between about 450 psi and about 1,000 psi (e.g., betweenabout 500 psi and about 900 psi, between about 600 psi and about 800psi, etc.).

In some embodiments, board made according to the invention meets testprotocols according to ASTM Standard C473-10. For example, in someembodiments, when the board is cast at a thickness of V inch, the boardhas a nail pull resistance of at least about 65 lb as determinedaccording to ASTM C473-10, e.g., at least about 68 lb, at least about 70lb, at least about 72 lb, at least about 75 lb, at least about 77 lb,etc. In various embodiments, the nail pull resistance can be from about68 lb to about 100 lb, e.g., from about 68 lb to about 95 lb, from about68 lb to about 90 lb, from about 68 lb to about 85 lb, from about 68 lbto about 80 lb, from about 68 lb to about 77 lb, from about 68 lb toabout 75 lb, from about 68 lb to about 72 lb, from about 68 lb to about70 lb, from about 70 lb to about 100 lb. from about 70 lb to about 95lb, from about 70 lb to about 90 lb, from about 70 lb to about 85 lb,from about 70 lb to about 80 lb, from about 70 lb to about 77 lb, fromabout 70 lb to about 75 lb, from about 70 lb to about 72 lb, from about72 lb to about 100 lb, from about 72 lb to about 95 lb, from about 72 lbto about 90 lb, from about 72 lb to about 85 lb, from about 72 lb toabout 80 lb, from about 72 lb to about 77 lb, from about 72 lb to about75 lb, from about 75 lb to about 100 lb, from about 75 lb to about 95lb, from about 75 lb to about 90 lb, from about 75 lb to about 85 lb,from about 75 lb to about 80 lb, from about 75 lb to about 77 lb, fromabout 77 lb to about 100 lb, from about 77 lb to about 95 lb, from about77 lb to about 90 lb, from about 77 lb to about 85 lb, or from about 77lb to about 80 lb.

With respect to flexural strength, in some embodiments, when cast in aboard of ½ inch thickness, the board has a flexural strength of at leastabout 36 lb in a machine direction (e.g., at least about 38 lb, at leastabout 40 lb, etc) and/or at least about 107 lb (e.g., at least about 110lb, at least about 112 lb, etc) in a cross-machine direction asdetermined according to the ASTM standard C473. In various embodiments,the board can have a flexural strength in a machine direction of fromabout 36 lb to about 60 lb, e.g., from about 36 lb to about 55 lb, fromabout 36 lb to about 50 lb, from about 36 lb to about 45 lb, from about36 lb to about 40 lb, from about 36 lb to about 38 lb, from about 38 lbto about 60 lb, from about 38 lb to about 55 lb, from about 38 lb toabout 50 lb, from about 38 lb to about 45 lb, from about 38 lb to about40 lb, from about 40 lb to about 60 lb, from about 40 lb to about 55 lb,from about 40 lb to about 50 lb, or from about 40 lb to about 45 lb. Invarious embodiments, the board can have a flexural strength in across-machine direction of from about 107 lb to about 130 lb, e.g., fromabout 107 lb to about 125 lb, from about 107 lb to about 120 lb, fromabout 107 lb to about 115 lb, from about 107 lb to about 112 lb, fromabout 107 lb to about 110 lb, from about 110 lb to about 130 lb, fromabout 110 lb to about 125 lb, from about 110 lb to about 120 lb, fromabout 110 lb to about 115 lb, from about 110 lb to about 112 lb, fromabout 112 lb to about 130 lb, from about 112 lb to about 125 lb, fromabout 112 lb to about 120 lb, or from about 112 lb to about 115 lb.

In addition, in some embodiments, board can have an average corehardness of at least about 11 lb, e.g., at least about 12 lb, at leastabout 13 lb, at least about 14 lb, at least about 15 lb, at least about16 lb, at least about 17 lb, at least about 18 lb, at least about 19 lb,at least about 20 lb, at least about 21 lb, or at least about 22 lb, asdetermined according to ASTM C473-10. In some embodiments, board canhave a core hardness of from about 11 lb to about 25 lb, e.g., fromabout 11 lb to about 22 lb, from about 11 lb to about 21 lb, from about11 lb to about 20 lb, from about 11 lb to about 19 lb, from about 11 lbto about 18 lb, from about 11 lb to about 17 lb, from about 11 lb toabout 16 lb, from about 11 lb to about 15 lb. from about 11 lb to about14 lb, from about 11 lb to about 13 lb, from about 11 lb to about 12 lb,from about 12 lb to about 25 lb, from about 12 lb to about 22 lb. fromabout 12 lb to about 21 lb, from about 12 lb to about 20 lb, from about12 lb to about 19 lb, from about 12 lb to about 18 lb, from about 12 lbto about 17 lb, from about 12 lb to about 16 lb, from about 12 lb toabout 15 lb, from about 12 lb to about 14 lb, from about 12 lb to about13 lb, from about 13 lb to about 25 lb, from about 13 lb to about 22 lb,from about 13 lb to about 21 lb, from about 13 lb to about 20 lb, fromabout 13 lb to about 19 lb, from about 13 lb to about 18 lb, from about13 lb to about 17 lb, from about 13 lb to about 16 lb, from about 13 lbto about 15 lb, from about 13 lb to about 14 lb, from about 14 lb toabout 25 lb, from about 14 lb to about 22 lb, from about 14 lb to about21 lb, from about 14 lb to about 20 lb, from about 14 lb to about 19 lb,from about 14 lb to about 18 lb, from about 14 lb to about 17 lb, fromabout 14 lb to about 16 lb, from about 14 lb to about 15 lb, from about15 lb to about 25 lb, from about 15 lb to about 22 lb, from about 15 lbto about 21 lb, from about 15 lb to about 20 lb, from about 15 lb toabout 19 lb, from about 15 lb to about 18 lb, from about 15 lb to about17 lb, from about 15 lb to about 16 lb, from about 16 lb to about 25 lb,from about 16 lb to about 22 lb, from about 16 lb to about 21 lb, fromabout 16 lb to about 20 lb, from about 16 lb to about 19 lb, from about16 lb to about 18 lb, from about 16 lb to about 17 lb, from about 17 lbto about 25 lb, from about 17 lb to about 22 lb, from about 17 lb toabout 21 lb, from about 17 lb to about 20 lb, from about 17 lb to about19 lb, from about 17 lb to about 18 lb, from about 18 lb to about 25 lb,from about 18 lb to about 22 lb, from about 18 lb to about 21 lb, fromabout 18 lb to about 20 lb, from about 18 lb to about 19 lb, from about19 lb to about 25 lb, from about 19 lb to about 22 lb, from about 19 lbto about 21 lb, from about 19 lb to about 20 lb, from about 21 lb toabout 25 lb, from about 21 lb to about 22 lb. or from about 22 lb toabout 25 lb.

Due at least in part to the mid-range viscosity characteristic thatresults in some embodiments of the invention, these standards (e.g.,nail pull resistance, flexural strength, and core hardness) can be meteven with respect to ultra light density board (e.g., about 31 pcf orless) as described herein.

It has also been found by the inventors that pregelatinized, partiallyhydrolyzed starches prepared in accordance with embodiments of theinvention demonstrate temperature rise set (TRS) hydration rates thatare comparable to or surpass those of conventional pregelatinizedstarches prepared according to a different method. The desired settingtime may depend on the formulation, and the desired setting time can bedetermined by one of ordinary skill in the art depending on plantconditions and available raw materials.

Product according to embodiments of the invention can be made on typicalmanufacturing lines. For example, board manufacturing techniques aredescribed in, for example, U.S. Pat. No. 7,364,676 and U.S. PatentApplication Publication 2010/0247937. Briefly, in the case of gypsumboard, the process typically involves discharging a cover sheet onto amoving conveyor. Since gypsum board is normally formed “face down,” thiscover sheet is the “face” cover sheet in such embodiments.

Dry and/or wet components of the gypsum slurry are fed to a mixer (e.g.,pin mixer), where they are agitated to form the gypsum slurry. The mixercomprises a main body and a discharge conduit (e.g., agate-canister-boot arrangement as known in the art, or an arrangement asdescribed in U.S. Pat. Nos. 6,494,609 and 6,874,930). In someembodiments, the discharge conduit can include a slurry distributor witheither a single feed inlet or multiple feed inlets, such as thosedescribed in U.S. Patent Application Publication 2012/0168527 A1(application Ser. No. 13/341,016) and U.S. Patent ApplicationPublication 2012/0170403 A1 (application Ser. No. 13/341,209), forexample. In those embodiments, using a slurry distributor with multiplefeed inlets, the discharge conduit can include a suitable flow splitter,such as those described in U.S. Patent Application Publication2012/0170403 A1. Foaming agent can be added in the discharge conduit ofthe mixer (e.g., in the gate as described, for example, in U.S. Pat.Nos. 5,683,635 and 6,494,609) or in the main body if desired. Slurrydischarged from the discharge conduit after all ingredients have beenadded, including foaming agent, is the primary gypsum slurry and willform the board core. This board core slurry is discharged onto themoving face cover sheet.

The face cover sheet may bear a thin skim coat in the form of arelatively dense layer of slurry. Also, hard edges, as known in the art,can be formed, e.g., from the same slurry stream forming the face skimcoat. In embodiments where foam is inserted into the discharge conduit,a stream of secondary gypsum slurry can be removed from the mixer bodyto form the dense skim coat slurry, which can then be used to form theface skim coat and hard edges as known in the art. If included, normallythe face skim coat and hard edges are deposited onto the moving facecover sheet before the core slurry is deposited, usually upstream of themixer. After being discharged from the discharge conduit, the coreslurry is spread, as necessary, over the face cover sheet (optionallybearing skim coat) and covered with a second cover sheet (typically the“back” cover sheet) to form a wet assembly in the form of a sandwichstructure that is a board precursor to the final product. The secondcover sheet may optionally bear a second skim coat, which can be formedfrom the same or different secondary (dense) gypsum slurry as for theface skim coat, if present. The cover sheets may be formed from paper,fibrous mat or other type of material (e.g., foil, plastic, glass mat,non-woven material such as blend of cellulosic and inorganic filler,etc.).

The wet assembly thereby provided is conveyed to a forming station wherethe product is sized to a desired thickness (e.g., via forming plate),and to one or more knife sections where it is cut to a desired length.The wet assembly is allowed to harden to form the interlockingcrystalline matrix of set gypsum, and excess water is removed using adrying process (e.g., by transporting the assembly through a kiln).Surprisingly and unexpectedly, it has been found that board preparedaccording to the invention with pregelatinized, partially hydrolyzedstarch prepared in accordance with embodiments of the invention requiressignificantly less time in a drying process because of the low waterdemand characteristic of the starch. This is advantageous because itreduce energy costs.

It also is common in the manufacture of gypsum board to use vibration inorder to eliminate large voids or air pockets from the deposited slurry.Each of the above steps, as well as processes and equipment forperforming such steps, are known in the art.

The pregelatinized, partially hydrolyzed starch prepared in accordancewith embodiments of the invention can be used in formulating variousproducts, such as, for example, gypsum wallboard, acoustical (e.g.,ceiling) tile, joint compound, gypsum-cellulosic fiber products, such asgypsum-wood fiber wallboard, and the like. In some embodiments, suchproduct can be formed from slurry according to embodiments of theinvention.

As such, pregelatinized, partially hydrolyzed starch prepared in anextruder in accordance with embodiments of the invention can havebeneficial effect, as described herein, in product besides paper-facedgypsum board in embodiments of the invention. For example,pregelatinized, partially hydrolyzed starch prepared in accordance withembodiments of the invention can be used in mat-faced products (e.g.,woven) where board cover sheets are in the form of fibrous mats. Themats can optionally bear a finish to reduce water permeability. Otheringredients that can be included in making such mat-faced product, aswell as materials for the fibrous mats and methods of manufacture, arediscussed in, e.g., U.S. Pat. No. 8,070,895, as well as U.S. PatentApplication Publication 2009/0247937,

In addition, gypsum-cellulosic product can be in the form of cellulosichost particles (e.g., wood fibers), gypsum, pregelatinized, partiallyhydrolyzed starch prepared in accordance with embodiments of theinvention, and other ingredients (e.g., water resistant additives suchas siloxanes) as desired. Other ingredients and methods of manufactureare discussed in, e.g., U.S. Pat. Nos. 4,328,178; 4,239,716; 4,392,896;4,645,548; 5,320,677; 5,817,262; and 7,413,603.

ILLUSTRATIVE EXAMPLES OF EMBODIMENTS

In one embodiment, a method of making a pregelatinized, partiallyhydrolyzed starch comprises: (a) mixing at least water,non-pregelatinized starch, and a weak acid that substantially avoidschelating calcium ions to make a wet starch precursor having a moisturecontent of from about 8 wt. % to about 25 wt. %; (b) feeding the wetstarch precursor into an extruder; and (c) pregelatinizing andacid-modifying the wet starch precursor in the extruder at a dietemperature of about 150° C. (about 300° F.) to about 210° C. (about410° F.).

In another embodiment, the pressure inside the extruder is at leastabout 2,000 psi.

In another embodiment, the pregelatinized, partially hydrolyzed starchhas a cold water solubility greater than about 50%.

In another embodiment, the pregelatinized, partially hydrolyzed starchhas a cold water viscosity (10% solids, 25° C.) of from about 10Brabender Unit (BU) to about 120 BU.

In another embodiment, the pregelatinized, partially hydrolyzed starchhas a viscosity characteristic of from about 20 centipoise to about 700centipoise when the viscosity is measured while the starch is subjectedto the conditions according to the VMA method.

In another embodiment, the pregelatinized, partially hydrolyzed starchhas a viscosity (10% solids, 93° C.) of from about 5 BU to about 33 BU.

In another embodiment, the weak acid that substantially avoids chelatingcalcium ions comprises alum.

In another embodiment, tartaric acid is included in the mixing to formthe wet starch precursor.

In another embodiments, the weak acid that substantially avoidschelating calcium ions is in an amount of from about 0.5 wt. % to about5 wt. % by weight of the starch.

In another embodiment, the wet starch has a moisture content of fromabout 10 wt. % to about 20 wt. % by weight of the starch precursor.

In another embodiment, the pregelatinizing and acid-modifying occurs ata die temperature of from at least about 175° C. (about 350° F.) toabout 205° C. (about 400° F.) in the extruder.

In another embodiment, the output of the pregelatinized, partiallyhydrolyzed starch is at least about 100 kg/hr in the extruder.

In another embodiment, the pregelatinizing and acid-modifying occurs inless than about 5 minutes.

In another embodiment, the pregelatinizing and acid-modifying occurs inless than about 1 minute.

In another embodiment, the method is free of a purification step for thepregelatinized, partially hydrolyzed starch.

In another embodiment, the method is free of a neutralization step forthe pregelatinized, partially hydrolyzed starch.

In another embodiment, the pregelatinized, partially hydrolyzed starchis at least about 70% gelatinized.

In another embodiment, a pregelatinized, partially hydrolyzed starch isprepared according to embodiments of the invention.

In another embodiment, a method of making a pregelatinized, partiallyhydrolyzed starch comprises: (a) mixing at least water,non-pregelatinized starch, and a strong acid to make a wet starchprecursor having a moisture content of from about 8 wt. % to about 25wt. %, wherein the strong acid is in an amount of about 0.05 wt. % orless by weight of the starch; (b) feeding the wet starch precursor intoan extruder; and (c) pregelatinizing and acid-modifying the wet starchin the extruder at a die temperature of about 150° ((about 300° F.) toabout 210° C. (about 410° F.).

In another embodiment, a method of making a pregelatinized, partiallyhydrolyzed starch comprises: (a) mixing at least water,non-pregelatinized starch, and a strong acid to make a wet starchprecursor having a moisture content of from about 8 wt. % to about 25wt. %, wherein the strong acid is in an amount of about 0.01 wt. % orless by weight of the starch; (b) feeding the wet starch precursor intoan extruder; and (c) pregelatinizing and acid-modifying the wet starchin the extruder at a die temperature of about 150° C. (about 300° F.) toabout 210° C. (about 410° F.).

In another embodiment, the strong acid has a pKa of about −1.7 or less.

In another embodiment, the strong acid is sulfuric acid, nitric acid,hydrochloric acid, or any combination thereof.

In another embodiment, the method of making board comprises: (a) forminga pregelatinized, partially hydrolyzed starch by (i) mixing at leastwater, non-pregelatinized starch, and an acid to form a wet starchprecursor having a moisture content of from about 8 wt. % to about 25wt. %, the acid selected from the group consisting of: (1) a weak acidthat substantially avoids chelating calcium ions, (2) a strong acid inan amount of about 0.05 wt. % or less by weight of the starch, or (3)any combination thereof; (ii) feeding the wet starch precursor into anextruder; and (iii) pregelatinizing and acid-modifying the wet starch inthe extruder having a die at a temperature of about 150° C. (about 300°F.) to about 210° C. (about 410° F.); (b) mixing the pregelatinized andpartially hydrolyzed starch with at least water and stucco to form aslurry; (c) disposing the slurry between a first cover sheet and asecond cover sheet to form a wet assembly; (d) cutting the wet assemblyinto a board; and (e) drying the board.

In another embodiment, the strong acid is in an amount of about 0.01 wt.% or less by weight of the starch.

In another embodiment, a method of making board comprises (a) forming apregelatinized, partially hydrolyzed starch by (i) mixing at leastwater, non-pregelatinized starch, and a weak acid that substantiallyavoids chelating calcium ions to make a wet starch precursor having amoisture content of from about 8 wt. % to about 25 wt. %; (ii) feedingthe wet starch into an extruder; and (iii) pregelatinizing andacid-modifying the wet starch in an extruder having a die at atemperature of about 150° C. (about 300° F.) to about 210° C. (about410° F.); (b) mixing the pregelatinized and partially hydrolyzed starchwith at least water and stucco to form a slurry; (c) disposing theslurry between a first cover sheet and a second cover sheet to form awet assembly; (d) cutting the wet assembly into a board; and (e) dryingthe board.

In another embodiment, the method of making board comprises: (a) mixingat least water, non-pregelatinized starch, and a strong acid to make awet starch precursor having a moisture content of from about 8 wt. % toabout 25 wt. %, wherein the strong acid is in an amount of about 0.05wt. % or less by weight of the starch; (ii) feeding the wet starchprecursor into an extruder; and (iii) pregelatinizing and acid-modifyingthe wet starch in the extruder having a die at a temperature of about150° C. (about 300° F.) to about 210° C. (about 410° F.); (b) mixing thepregelatinized and partially hydrolyzed starch with at least water andstucco to form a slurry; (c) disposing the slurry between a first coversheet and a second cover sheet to from a wet assembly; (d) cutting thewet assembly into a board; and (e) drying the board.

In another embodiment, the strong acid is in an amount of about 0.01 wt.% or less by weight of the starch.

In another embodiment, the set gypsum core has a compressive strengthgreater than a set gypsum core made with a starch prepared under adifferent method.

In another embodiment, the pregelatinized, partially hydrolyzed starchis at least about 70% gelatinized when added to the slurry, withadditional gelatinization taking place in the drying step.

In another embodiment, the pregelatinized, partially hydrolyzed starchis fully gelatinized when added to the slurry.

In another embodiment, the board has a compressive strength of at leastabout 400 psi (2,800 kPa) at a density of 29 pcf.

In another embodiment, the board has a core hardness of at least about11, as determined according to ASTM C473-10.

In another embodiment, the board has a density of from about 21 pcf toabout 35 pcf.

In another embodiment, the slurry further comprises sodiumtrimetaphosphate.

In another embodiment, the amount of water needed to be added tomaintain the slurry fluidity at the same level it would be without thepregelatinized, partially hydrolyzed starch, is less than the increasein the amount of water needed when using a pregelatinized, partiallyhydrolyzed starch prepared according to a different method.

In another embodiment, the starch is in an amount of from about 0.5% toabout 10% by weight based on the weight of the stucco.

In another embodiment, a wallboard is prepared according to embodimentsof the invention.

It shall be noted that the preceding are merely examples of embodiments.Other exemplary embodiments are apparent from the entirety of thedescription herein. It will also be understood by one of ordinary skillin the art that each of these embodiments may be used in variouscombinations with the other embodiments provided herein.

The following examples further illustrate the invention but, of course,should not be construed as in any way limiting its scope.

Example 1

This Example illustrates the preparation of pregelatinized, partiallyhydrolyzed starches in accordance with embodiments of the invention.

Nine pregelatinized, partially hydrolyzed starches prepared inaccordance with embodiments of the invention were prepared for varioustests of specific properties (e.g., viscosity, fluidity, strength).These nine inventive starches were tested alongside three commerciallyavailable starches.

In accordance with the inventive method of preparing pregelatinized,partially hydrolyzed starch, wet starch precursors were prepared bymixing a determined corn flour commercially available as CCM 260 YellowCorn Meal from Bunge North America (St. Louis, Mo.) in an amount of 100kg, varying amounts of aluminum sulfate (alum), a weak acid thatsubstantially avoids chelating with calcium ions, and/or tartaric acid(less than 20 wt. % of the total of weak acids), and varying amounts ofwater. The wet starch precursors were fed into a single screw extrudercommercially available as Advantage 50 from American ExtrusionInternational (South Beloit, Ill.). In the extruder, the wet starchprecursors were pregelatinized and acid-modified in a single step, suchthat they occurred simultaneously.

Table 4 below describes the parameters of the extrusion of the cornflour in the presence of acid. The residence time of extrusion (i.e.,the time for pregelatinization and acid-modification) was less than 30seconds. All percents are based on the total weight of the starch,except moisture, which is based on the total wet weight, expressed asthe sum of water, starch, and other additives.

The resulting pregelatinized, partially hydrolyzed starches wereevaluated against a conventional pregelatinized corn starch having aviscosity of 773 centipoise designated Composition 1A (comparative), aswell as two low water-demand starches prepared by extrusion ofacid-modified corn starches, commercially available as Clinton 277 (ADM,Chicago, Ill.) and Caliber 159 (Cargill, Wayzata, Minn.), designatedComposition 1B (comparative) and Composition 1C (comparative),respectively.

TABLE 4 Substrate Corn Flour Canola oil 0.25 wt. % Liquid alum 1 wt. %-4wt. % Tartaric acid  0 wt. %-0.3 wt. % Moisture of starch duringextrusion 10 wt. %-20 wt. % Main screw (RPM) 350 Feed auger speed (RPM) 14 Die temperature (° F.) 350-370 Knife speed (RPM)  400-1,000

Pregelatinized, partially hydrolyzed starches, designated Compositions1D-1L, were produced in the extrusion process.

Table 5 below details the various moisture contents for extrusion andacid contents during extrusion for Compositions 1D-1L. Compositions1D-1H and 1L were prepared with a moisture content of 16 wt. %, whileCompositions 1I-1K were prepared with a moisture content of 13 wt. %.Compositions 1D-1G and Compositions 1I-1L were prepared with liquid alumin an amount of ranging from 1 wt. % to 4 wt. %, while Composition 1Hincluded liquid alum and tartaric acid. Compositions 1F and 1L wereprepared using the same moisture content and amount of acid, but inExample 3 had different amounts of retarder.

TABLE 5 Composition Moisture Acid Composition 1A 16 wt. % NA Composition1B 19 wt. % NA Composition 1C 19 wt. % NA Composition 1D 16 wt. % 1 wt.% alum Composition 1E 16 wt. % 2 wt. % alum Composition 1F 16 wt. % 3wt. % alum Composition 1G 16 wt. % 4 wt. % alum Composition 1H 16 wt. %2 wt. % alum; 0.3 wt. % tartaric acid Composition 1I 13 wt. % 1 wt. %alum Composition 1J 13 wt. % 2 wt. % alum Composition 1K 13 wt. % 3 wt.% alum Composition 1L 16 wt. % 3 wt. % alum

Examples 2-4 below test the Compositions described in Table 5 forvarious properties. In Example 2, Compositions 1B-1L were evaluated withregards to viscosity in amylograph tests. Example 3 tested slurriesprepared with one of Compositions 1A, 1D-1I, and 1K-1L for fluidity,which was evaluated by means of a slump test. This data was then furthercorroborated by measuring the time to 50% hydration for the slurries.This illustrated how much time it took for the slurries to set. Example4 tested slurries prepared with Compositions 1A, 1D-1I, and 1K forstrength, which was evaluated by means of a compressive strength testdescribed herein.

Example 2

This example illustrates the viscosity of pregelatinized, partiallyhydrolyzed starches prepared in an extruder in accordance withembodiments of the invention. Compositions 1D-1K were tested incomparison to extruded commercially available acid-modified starches(Compositions 1B-1C), specifically with regards to how viscosity changesbased on the amount of acid (e.g., alum) and moisture content, definedby the level of moisture of the wet starch that is fed through theextruder.

In preparation for testing, the Compositions were mixed with water intoa starch slurry, such that the starch slurries contained theCompositions in an amount of 10 wt. %. It will be noted that the term“solution” is used when the starch is fully gelatinized and completelydissolved and the term “slurry” is used when the starch is notcompletely dissolved. Each Composition was then tested for viscosity atdifferent temperatures by the Amylograph technique described herein. Theresults of the tests were plotted in FIGS. 1 and 2, which are amylogramsevaluating the viscosity of pregelatinized, partially hydrolyzedstarches at different temperatures by plotting viscosity (left y-axis)and temperature (right y-axis) versus time (x-axis). The temperaturecurve is overlaid against each sample. The same temperature profile wasused for each sample. The other curves show the viscosity of thestarches.

The initial viscosity at 25° C. was an indicator of the fluidity of aslurry system containing any one of Compositions 1B-1K. 25° C. is thetemperature at which the starch will be mixed with stucco and otheringredients to make board. At this temperature, furthermore, theviscosity of the starch is negatively correlated with the fluidity ofthe stucco slurry.

The viscosity at trough (93° C.) was an indicator of the molecularweight of any one of Compositions 1B-1K. At a temperature of 93° C., thestarch molecules are completely dissolved in water. The viscosity of thestarch solutions at 93° C. is positively correlated with the molecularweight of the starch, which results from partial hydrolysis.

FIG. 1 is an amylogram plotting viscosity (left y-axis) and temperature(right y-axis) over a fifty minute period (x-axis). ComparativeCompositions 1B and 1C and inventive Compositions 1D-1H, as describedherein, were mixed into starch solutions in an amount of 10% by weightbased on the weight of the solution. To avoid forming lumps, starch wasadded into the water in a mixing cup of a Waring blender while mixed atlow speed for 20 seconds. The starch solutions were then evaluated usinga Viscograph-E (C. W. Brabender® Instruments, Inc., South Hackensack,N.J.). According to the Brabender viscosity measurement procedure asreferred to herein, viscosity is measured using a C. W. BrabenderViscograph, e.g., a Viscograph-E that uses reaction torque for dynamicmeasurement. It is to be noted that, as defined herein, the Brabenderunits are measured using a sample cup size of 16 fl. oz (about 500 cc),with a 700 cmg cartridge at an RPM of 75. One of ordinary skill in theart also will readily recognize that the Brabender units can beconverted to other viscosity measurements, such as centipoises (e.g.,cP=BU×2.1, when the measuring cartridge is 700 cmg) or Krebs units, asdescribed therein. The pasting profiles of Compositions 1D-1H extrudedat 16 wt. % moisture content are shown in FIG. 1 along with comparativeCompositions 1B and 1C.

Considering inventive Compositions 1D-1H, as alum increased from 1 wt. %to 4 wt. %, the initial viscosity decreased from 70 Brabender Unit (BU)to 10 BU, while the molecular weight decreased as well. The initialviscosities and viscosities at 93° C. of Compositions 1D-1H were reducedas low as those of Compositions 1B and 1C. Compositions 1B and 1Crepresent conventional viscosity limits of low water demand starches.

The results of Compositions 1D-1H shown in FIG. 1 demonstrate thatoptimal acid-modification can be achieved during extrusion. Theseresults further suggest that the inventive method of preparingpregelatinized, partially hydrolyzed starch successfully reduced theviscosity (molecular weight) of the starch. No viscosity peak wasobserved between 70C to 90° C., indicating that Compositions 1D-1H werefully gelatinized. Had Compositions 1D-1H not been fully gelatinized,there would have been an increase in viscosity. The full gelatinizationof the starch Compositions were confirmed by differential scanningcalorimetry (DSC).

FIG. 2 is a second amylogram plotting viscosity (left y-axis) andtemperature (right y-axis) over a fifty minute period (x-axis).Comparative Compositions 1B and 1C and inventive Compositions 1I-1K, allas described herein, were mixed into starch solutions in an amount of10% by weight based on the weight of the solution. To avoid forminglumps, starch was added into the water in a mixing cup of a Waringblender while mixed at low speed for 20 seconds. The starch solutionswere then evaluated using a Viscograph-E. The pasting profiles ofCompositions 1I-1K extruded at 13 wt. % moisture content are shown inFIG. 2 along with comparative Compositions 1B and 1C.

Similar trends observed with Compositions 1D-1H were observed withCompositions 1I-1K. In particular, the method of preparingpregelatinized, partially hydrolyzed starch in an extruder as describedherein successfully reduced the viscosity of Compositions 1I-1K.

As alum increased from 1 wt. % to 3 wt. %, the initial viscositydecreased from 75 BU to 14 BU, while the molecular weight alsodecreased. The initial viscosities and the viscosity at 93° C. ofCompositions 1I-1K were reduced as low as those of Compositions 1B and1C.

In addition, the results of Compositions 1I-1K shown in FIG. 2demonstrate that optimal acid-modification can be achieved duringextrusion. No viscosity peak was observed between 70° C. to 90° C.indicating that Compositions 1I-1K were fully gelatinized.

Furthermore, these results show that at a lower moisture content, morestarch hydrolysis can be achieved at a given acid level than at a highermoisture content because at a low moisture content there is moremechanical energy and, thus, more starch degradation, such that thestarch will become smaller using the same acid level.

Example 3

This Example illustrates the fluidity of gypsum slurries containingCompositions 1A (comparative), 1D-1I, and 1K-1L. The Compositions wereevaluated with regards to fluidity using a slump test that will beappreciated by one of ordinary skill in the art.

In preparation for testing, slurries were prepared with each ofCompositions 1A (comparative), 1D-1I, and 1K-1L in an amount of 2 wt. %and the parameters outlined in Table 6 below, using a water stucco ratio(WSR) of 100.

TABLE 6 Ingredient Weight (g) Stucco 400 Heat resistance accelerator 4Starch 8 Sodium trimetaphosphate 10% solution 8 Dispersant 2 Retarder 1%solution 20 Gauging water 357 PFM-33 foam (0.5% solution) 25

The starch was weighed into a dry mix comprising stucco having over 95%purity and heat resistance accelerator. Water, sodium trimetaphosphate(10 wt. % solution), dispersant, and retarder were weighed into themixing bowl of a Hobart Mixer. The dry mix was poured into the mixingbowl of a mixer available as N50 5-Quart Mixer from Hobart (Troy, Ohio),soaked for 10 seconds, and mixed at speed II for 30 seconds. For foampreparation, a 0.5% solution of Hyonic® PFM-33 soap (available from GEO®Specialty Chemicals, Ambler, Pa.) was formed, and then mixed with air tomake the air foam. The air foam was added to the slurry using a foamgenerator.

Each slurry was then put into a cylinder, having a diameter of 4.92 cm(1.95 in.) and a height of 10 cm (3.94 in.). The cylinder was thenlifted, allowing the slurry to freely flow. The diameters of the slumpsthat formed were then measured to illustrate fluidity of the slurriesand are recorded in Table 7 below. Table 8 also includes the results ofa time to 50% hydration test explained in further detail below.

TABLE 7 Time to 50% Hydration Composition Retarder Slump (cm) (minutes)Composition 1A 0.05 wt. % 13.7 cm (5⅜ in) 4 Composition 1D 0.05 wt. %16.5 cm (6½ in) 3.8 Composition 1E 0.05 wt. % 15.2 cm (6 in) 3.6Composition 1F 0.05 wt. % 16.2 cm (6⅜ in) 3.7 Composition 1G 0.05 wt. %16.2 cm (6⅜ in) 3.3 Composition 1H 0.05 wt. % 17.8 cm (7 in) 3.7Composition 1I 0.05 wt. % 15.9 cm (6¼ in) 3.6 Composition 1K 0.05 wt. %18.4 cm (7¼ in) 3.4 Composition 1L 0.0625 wt. %  18.4 cm (7¼ in) 4

As can be observed from Table 7, slurries prepared with Compositions1D-1I and 1K showed larger slump sizes than the slurry prepared withComposition 1A (comparative). They also set faster than Composition 1A(comparative), indicating slurries containing Compositions 1D-1I and 1Khad better fluidity than the slurry containing Composition 1A.

In addition, the time to 50% hydration was measured for the slurries forpurposes of comparing the slump size when the slurries set at the samerate. The temperature profiles of the slurries were measured usingsoftware as one of ordinary skill in the art will appreciate.

This additional test was conducted to confirm that the slump tests werecorrect, specifically to illustrate that the large slumps observed withslurries including pregelatinized, partially hydrolyzed starchesprepared in accordance with embodiments of the invention resulted fromimproved fluidity in comparison to Composition 1A (comparative), notslow hydration.

Composition 1H, prepared with 2 wt. % alum and 0.3 wt. % tartaric acid,effectively hydrolyzed starch to a low viscosity and had less impact onthe hydration rate, because tartaric acid and alum had opposite effecton hydration rate.

FIG. 3 is a graph plotting temperature versus time, showing thetemperature rise set (TRS) hydration rate. Compositions 1F with 0.05%and 0.0625% of retarder, respectively, hydrate faster or at the samerate as Composition 1A (comparative).

As seen in FIG. 3, Composition 1L, with 0.0625 wt. % of retarder, hadthe same hydration rate as Composition 1A (comparative). The slump sizeof Composition 1L with 0.065 wt. % retarder was 18.415 cm (7¼″), wassignificantly larger than Composite 1A.

This result suggests that the larger slump sizes observed with slurriesincluding pregelatinized, partially hydrolyzed starches prepared inaccordance with embodiments of the invention were due to high fluidityand not to slower setting. Furthermore, pregelatinized, partiallyhydrolyzed starches prepared in accordance with embodiments of theinvention will allow for wallboards using less water without sacrificingfluidity.

Example 4

This Example illustrates the strength of gypsum disks prepared withslurries containing Compositions 1A (comparative), 1D-1I, and 1K.Strength was evaluated using a compressive strength test describedherein.

To prepare for testing, slurries were prepared with each of Compositions1A (comparative), 1D-1I, and 1K-1L in an amount of 2 wt. % and theparameters outlined in Table 4 above.

A water stucco ratio (WSR) of 100 and air foam were used to make gypsumdisks with a final density of 29 pcf. The starch was weighed into a drymix comprising stucco and heat resistance accelerator. Water, sodiumtrimetaphosphate 10% solution, dispersant, and retarder were weighedinto the mixing bowl of a Hobart Mixer. The dry mix was poured into themixing bowl of a mixer available as N50 5-Quart Mixer from Hobart (Troy,Ohio), soaked for 10 seconds, and mixed at speed II for 30 seconds. Forfoam preparation, a 0.5% solution of Hyonic® PFM-33 soap (available fromGEO® Specialty Chemicals, Ambler, Pa.) was formed, and then mixed withair to make the air foam. The air foam was added to the slurry using afoam generator. The foam generator was run at a rate sufficient toobtain the desired board density of 29 pcf. After foam addition, theslurry was immediately poured to a point slightly above the tops of themolds. The excess was scraped as soon as the plaster set. The molds hadbeen sprayed with mold release (WD-40™). The disks had a diameter of10.16 cm (4 in.) and a thickness of 1.27 cm (0.5 in.).

After the disks had hardened, the disks were removed from the mold, andthen dried at 110° F. (43° C.) for 48 hours. After removing from theoven, the disks were allowed to cool at room temperature for 1 hour. Thecompressive strength was measured using a materials testing systemcommercially available as SATEC™ E/M Systems from MTS SystemsCorporation (Eden Prairie, Minn.). The load was applied continuously andwithout a shock at speed of 0.04 inch/min (with a constant rate between15 to 40 psi/s). The results are shown in Table 8 below.

TABLE 8 Compressive Strength Composition (PSI@29 pcf) Composition 1A 396Composition 1D 439 Composition 1E 388 Composition 1F 476 Composition 1G419 Composition 1H 417 Composition 1I 455 Composition 1K 426

As seen in Table 8, the foam disks containing Compositions 1D-1I and 1Khad compressive strengths comparable to that which contained Composition1A (comparative), indicating pregelatinized, partially hydrolyzedstarches could reduce water demand without sacrificing their strengthenhancing property. The desirable compressive strength of the disksamples is approximate 400 psi. The strength is required so that theboard can be properly handled without falling apart.

The use of the terms “a” and “an” and “the” and “at least one” andsimilar referents in the context of describing the invention (especiallyin the context of the following claims) (e.g., in relation to acids, rawmaterial starches, or other components or items) are to be construed tocover both the singular and the plural, unless otherwise indicatedherein or clearly contradicted by context. The use of the term “at leastone” followed by a list of one or more items (for example, “at least oneof A and B”) is to be construed to mean one item selected from thelisted items (A or B) or any combination of two or more of the listeditems (A and B), unless otherwise indicated herein or clearlycontradicted by context. The terms “comprising,” “having,” “including,”and “containing” are to be construed as open-ended terms (i.e., meaning“including, but not limited to,”) unless otherwise noted. Recitation ofranges of values herein are merely intended to serve as a shorthandmethod of referring individually to each separate value falling withinthe range, unless otherwise indicated herein, and each separate value isincorporated into the specification as if it were individually recitedherein. All methods described herein can be performed in any suitableorder unless otherwise indicated herein or otherwise clearlycontradicted by context. The use of any and all examples, or exemplarylanguage (e.g., “such as”) provided herein, is intended merely to betterilluminate the invention and does not pose a limitation on the scope ofthe invention unless otherwise claimed. No language in the specificationshould be construed as indicating any non-claimed element as essentialto the practice of the invention.

Preferred embodiments of this invention are described herein, includingthe best mode known to the inventors for carrying out the invention.Variations of those preferred embodiments may become apparent to thoseof ordinary skill in the art upon reading the foregoing description. Theinventors expect skilled artisans to employ such variations asappropriate, and the inventors intend for the invention to be practicedotherwise than as specifically described herein. Accordingly, thisinvention includes all modifications and equivalents of the subjectmatter recited in the claims appended hereto as permitted by applicablelaw. Moreover, any combination of the above-described elements in allpossible variations thereof is encompassed by the invention unlessotherwise indicated herein or otherwise clearly contradicted by context.

1. A method of making a pregelatinized, partially hydrolyzed starchcomprising: (a) mixing at least water, non-pregelatinized starch, and astrong acid to make a wet starch precursor having a moisture content offrom about 8 wt. % to about 25 wt. %, wherein the strong acid is in anamount of about 0.05 wt. % or less by weight of the starch; (b) feedingthe wet starch precursor into an extruder; and (c) pregelatinizing andacid-modifying the wet starch precursor in the extruder at a dietemperature of about 150° C. to about 210° C., wherein thepregelatinized, partially hydrolyzed starch is at least about 70%gelatinized, and wherein the pregelatinized, partially hydrolyzed starchhas a cold water viscosity of from about 10 Brabender Unit (BU) to about120 BU, wherein the cold water viscosity is determined by the Amylographmethod for a 10% by weight solution of the starch at 25° C.
 2. Themethod of claim 1, wherein the strong acid has a pKa of about −1.7 orless.
 3. The method of claim 1, wherein the strong acid is sulfuricacid, nitric acid, hydrochloric acid, or any combination thereof.
 4. Themethod of claim 1, wherein the strong acid is sulfuric acid.
 5. Themethod of claim 1, wherein the strong acid is in an amount of from about0.0001 wt. % to about 0.02 wt. % of the non-pregelatinized starch. 6.The method of claim 5, wherein the strong acid is in an amount of fromabout 0.0001 wt. % to about 0.01 wt. % of the non-pregelatinized starch.7. The method of claim 1, wherein the pregelatinized, partiallyhydrolyzed starch has a hot water viscosity of from about 5 BrabenderUnit (BU) to about 33 BU for a 10% by weight solution of the starch at30 min and 93° C. determined by the Amylograph method.
 8. The method ofclaim 1, wherein the pregelatinizing and acid-modifying occurs at a dietemperature of from at least about 175° C. to about 205° C. in theextruder.
 9. The method of claim 1, wherein the output of thepregelatinized, partially hydrolyzed starch is at least about 100 kg/hrin the extruder.
 10. The method of claim 1, wherein the pregelatinizingand acid-modifying occurs in less than about 5 minutes.
 11. The methodof claim 1, wherein the pregelatinizing and acid-modifying occurs inless than about 1 minute.
 12. The method of claim 1, wherein the methodis free of purification and neutralization steps for the pregelatinized,acid-modified starch.
 13. A pregelatinized, partially hydrolyzed starchprepared according to claim
 1. 14. A method of making board comprising:(a) mixing at least water, non-pregelatinized starch, and a strong acidto make a wet starch precursor having a moisture content of from about 8wt. % to about 25 wt. %, wherein the strong acid is in an amount ofabout 0.05 wt. % or less by weight of the starch; (b) feeding the wetstarch precursor into an extruder; and (iii) pregelatinizing andacid-modifying the wet starch precursor in the extruder having a die ata temperature of about 150° C. to about 210° C., wherein thepregelatinized, partially hydrolyzed starch is at least about 70%gelatinized and wherein the pregelatinized, partially hydrolyzed starchhas a cold water viscosity of from about 10 Brabender Unit (BU) to about120 BU, wherein the cold water viscosity is determined by the Amylographmethod for a 10% by weight solution of the starch at 25° C.; (c) mixingthe pregelatinized and partially hydrolyzed starch with at least waterand stucco to form a slurry; (d) disposing the slurry between a firstcover sheet and a second cover sheet to form a wet assembly; (e) cuttingthe wet assembly into a board; and (f) drying the board.
 15. The methodof claim 14, wherein the strong acid is sulfuric acid, nitric acid,hydrochloric acid, or any combination thereof.
 16. The method of claim15, wherein the strong acid is sulfuric acid.
 17. The method of claim14, wherein the strong acid is in an amount of from about 0.0001 wt. %to about 0.02 wt. % of the non-pregelatinized starch.
 18. The method ofclaim 17, wherein the strong acid is in an amount of from about 0.0001wt. % to about 0.01 wt. % of the non-pregelatinized starch.
 19. Themethod of claim 14, wherein the pregelatinized, partially hydrolyzedstarch has a hot water viscosity of from about 5 Brabender Unit (BU) toabout 33 BU for a 10% by weight solution of the starch at 30 min and 93°C. determined by the Amylograph method.
 20. The method of claim 14,wherein the board has a density of from about 21 pcf to about 35 pcf.21. The method of claim 14, wherein the slurry further comprises sodiumtrimetaphosphate.
 22. A board prepared according to claim 14.